Latest recalls — page 25

Browse the most recent U.S. safety recalls in our connected official government data.

3,525 recalls in our current data. Showing 2,401–2,500, newest first.

NHTSA · Vehicle equipment · June 12, 2026

Waltco MDV Series Liftgate recall (26E034000)

A liftgate that falls unexpectedly increases the risk of injury.

Company / brand: Marion Body Works recalls

Official ID 26E034000 · Official record ↗

NHTSA · Vehicle · June 11, 2026

Altec AC Series Crane recall (26V384000)

Missing welds can lead to platform joint failure due to fatigue or overload, resulting in the platform falling from the boom tip, increasing the risk of injury.

Company / brand: Altec Industries recalls

Official ID 26V384000 · Official record ↗

NHTSA · Vehicle · June 11, 2026

Great Dane Champion recall (26V383000)

A liftgate that falls unexpectedly increases the risk of injury.

Company / brand: Great Dane Trailers recalls

Official ID 26V383000 · Official record ↗

NHTSA · Vehicle · June 11, 2026

International HV recall (26V382000)

A delayed brake release can increase the risk of crash.

Company / brand: International Motors recalls

Official ID 26V382000 · Official record ↗

CPSC · Consumer Product · June 11, 2026

Coffeemakers Recalled Due to Risk of Serious Injury from Burn Hazard; Imported by Kidisle

The recalled coffeemakers can become clogged, causing hot liquid or steam to build up and be released unexpectedly during use, posing a risk of serious injury from burn hazard.

Company / brand: ChangShaShiMengQiSiDianZiShangMaoYouXianGongSi recalls

Official ID 26557 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Yamaha Recalls UMAX Bistro and Bistro Deluxe Vehicles Due to Injury Hazard

The recalled Bistro and Bistro Deluxe vehicles have an inaccurate weight capacity certification label. This could result in the vehicle being overloaded, which poses an injury haza…

Company / brand: Yamaha Golf-Car Company recalls

Official ID 26556 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Houoto 642-2150V Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Prosperity goes straight up

The drain covers do not bear the required product markings, in violation of the mandatory safety standard under the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing ris…

Company / brand: Foshan Nanhai District Haichen Tengfei Hardware Factory recalls

Official ID 26555 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear

The recalled children's pajamas violate the mandatory flammability safety standard for children's sleepwear, posing a risk of serious burn injuries or death to children.

Company / brand: The Black Sheep Fam recalls

Official ID 26554 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Imported by California Innovations and Sold at Costco

The recalled coolers' latch magnet can detach, posing risk of serious injury or death from a choking hazard.

Company / brand: California Innovations recalls

Official ID 26553 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

7-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon.com by Hasuit Direct

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…

Company / brand: Shenzhen DUOMENGDUO Electronic Commerce Co recalls

Official ID 26552 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Nimood Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violate Mandatory Standard for Adult Portable Bed Rails

The recalled bed rails violate the mandatory standard for adult portable bed rails, because users can become entrapped within the bed rail or between the bed rail and the side of t…

Company / brand: shenzhenshinikezhinengshebeiyouxiangongsi (Shenzhen Nike Intelligent Equipment Co recalls

Official ID 26551 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Kawasaki Motors USA Recalls Model Year 2026 Teryx4 H2 and Teryx5 H2 Recreational Off-Road Vehicles Due to Impact and Injury Hazards

The drive converter sheave can break in certain circumstances, resulting in metal fragments being discharged within the engine compartment and surrounding area, posing impact and i…

Company / brand: Kawasaki Motors Manufacturing recalls

Official ID 26550 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Hopelight Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by MOCCI SHOP

The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…

Company / brand: Jiangsu Zhirun Xiangmu Management Co recalls

Official ID 26543 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Yamaha Recalls Model Year 2021-2022 Fleet Golf Cars Due to Risk of Serious Injury or Death from a Crash Hazard

The recalled golf cars' passenger-side brake cable could have been misrouted during assembly. If the cable was misrouted, abnormal wear can occur which can cause the passenger-side…

Company / brand: Yamaha Golf-Car Company recalls

Official ID 26542 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Timechee Changing Table Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Timechee

The recalled dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries or death to children. The dress…

Company / brand: Fujian Xiniuniu Home Furnishing Co recalls

Official ID 26541 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

School Specialty Recalls Tip Restraint Kits Included in Childcraft Furniture Due to Risk of Serious Injury or Death from Tip-Over Hazard

The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards. Should the defective plastic tip restra…

Company / brand: School Specialty recalls

Official ID 26540 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Merkury Innovations Recalls Hot + Cool Heating and Cooling Fans Due to Risk of Serious Injury or Death from Fire Hazard

The fan can overheat, posing a risk of serious injury or death from a fire hazard.

Company / brand: Merkury Innovations recalls

Official ID 26539 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

LiKee Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by ChilanTech

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's …

Company / brand: Guangzhou Huanmao Business Service Co recalls

Official ID 26538 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

HSN Recalls Kitchen HQ Thermal Insulated Bowls Due to Fire Hazard

Metal springs in the detachable hinged lid of the insulated bowls can catch fire when used in the microwave, posing a fire hazard.

Company / brand: HSN recalls

Official ID 26537 · Official notice ↗

CPSC · Consumer Product · June 11, 2026

Joyin Recalls Sloosh Dive Sticks Due to Risk of Serious Injury from Impalement; Violate Federal Dive Sticks Ban

The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a…

Company / brand: Joyin US recalls

Official ID 26536 · Official notice ↗

NHTSA · Vehicle · June 10, 2026

Denago EV Forward Collision Avoidance recall (26V381000)

A vehicle that does not emit sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.

Company / brand: Denago EV recalls

Official ID 26V381000 · Official record ↗

FDA Class I · Food · June 10, 2026

ANGEL branded STRAWBERRY SOFT-SERVE powder recall — SKS Copack

Products may potentially be contaminated with Salmonella.

Company / brand: SKS Copack recalls

Official ID EVT-99068-n58k06 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — Intuitive Surgical, Inc.

Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching fro…

Company / brand: Intuitive Surgical recalls

Official ID Z-2310-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Sharpoint 2 recall — SSC- Surgical Specialties Corporation

3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.

Company / brand: SSC- Surgical Specialties recalls

Official ID Z-2309-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

TITANIUM/FLUOROPLASTIC PISTON 0 recall — Grace Medical, Inc.

Due to incorrect functional length on device labeling.

Company / brand: Grace Medical recalls

Official ID Z-2308-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Aligned Medical AMS16835 Fluids Kit RX recall — Windstone Medical Packaging, Inc.

Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.

Company / brand: Windstone Medical Packaging recalls

Official ID Z-2307-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

MAC 5 A4 Resting ECG Analysis System 855001-001 recall — GE Medical Systems China Co., Ltd.

Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. …

Company / brand: GE Medical Systems China Co recalls

Official ID Z-2306-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

DeRoyal Industries Inc recall — DeRoyal Industries Inc

Sterile wound dressing, lacks sterility assurance

Company / brand: DeRoyal Industries recalls

Official ID Z-2305-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedBank Mini REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2304-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedBank Tower REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2303-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedStation ES Tower REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2302-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis Mini Main REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2301-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis Anesthesia Station 4000 REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2300-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis Anesthesia Station ES REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2299-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedStation ES REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2298-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

BD Pyxis MedStation 4000 REF recall — CareFusion 303, Inc.

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Company / brand: CareFusion 303 recalls

Official ID Z-2297-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the M recall — Bayer Medical Care, Inc.

Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock c…

Company / brand: Bayer Medical Care recalls

Official ID Z-2296-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Phothera 200 recall — Daavlin Distributing Company

Some of the Calibration/Output Certificates had the outputs reversed.

Company / brand: Daavlin Distributing Company recalls

Official ID Z-2295-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Digital Angiography System Trinias recall — Shimadzu Medical Systems

Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.

Company / brand: Shimadzu Medical Systems recalls

Official ID Z-2294-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Arvis Hip & Knee 2 recall — Kico Knee Innovation Company

The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.

Company / brand: Kico Knee Innovation Company recalls

Official ID Z-2293-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Arvis Hip & Knee 3 recall — Kico Knee Innovation Company

The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.

Company / brand: Kico Knee Innovation Company recalls

Official ID Z-2292-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 7M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2291-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 7M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2290-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 7B20/15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2289-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 7B12/12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2288-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 5M20 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2287-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 5M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2286-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 3M15 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2285-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Philips Azurion 3M12 recall — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…

Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls

Official ID Z-2284-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — Advanced Bionics, LLC

Due to incorrect shelf-life expiration date.

Company / brand: Advanced Bionics recalls

Official ID Z-2283-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Neptune Smart Docking Station (120V) recall — Stryker Corporation

It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being ship…

Company / brand: Stryker recalls

Official ID Z-2282-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien EndoStitch" Polysorb Single Use Loading Unit recall — Covidien, LP

The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.

Company / brand: Covidien recalls

Official ID Z-2281-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

CASE v7 recall — GE Medical Systems Information Technologies Inc

Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charr…

Company / brand: GE Medical Systems Information Technologies recalls

Official ID Z-2279-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall — B Braun Medical Inc

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…

Company / brand: B Braun Medical recalls

Official ID Z-2278-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Spinocan Spinal Needle procedure kits recall — B Braun Medical Inc

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…

Company / brand: B Braun Medical recalls

Official ID Z-2277-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Spinal Needle procedure kits recall — B Braun Medical Inc

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…

Company / brand: B Braun Medical recalls

Official ID Z-2276-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

PhaseOne Antimicrobial Solution recall — Oculus Technologies of Mexico, S.A. de C.V.

The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the produc…

Company / brand: Oculus Technologies of Mexico recalls

Official ID Z-2275-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC

Potential for the Cassette Loading Lever to break.

Company / brand: Fresenius Kabi USA recalls

Official ID Z-2274-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm general purpose temperature probe size recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Company / brand: Covidien recalls

Official ID Z-2273-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm General Purpose Temperature Probe REF recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Company / brand: Covidien recalls

Official ID Z-2272-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF recall — Covidien LLC

Temperature probe devices lack FDA clearance.

Company / brand: Covidien recalls

Official ID Z-2271-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2270-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2269-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2268-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2267-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2266-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2265-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2264-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — B Braun Medical Inc

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…

Company / brand: B Braun Medical recalls

Official ID Z-2263-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

Brand Name recall — Baxter Healthcare Corporation

Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slow…

Company / brand: Baxter Healthcare recalls

Official ID Z-2262-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code recall — Covidien LLC

Due to customer complaint regarding incorrect display box labeling.

Company / brand: Covidien recalls

Official ID Z-2261-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2257-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2256-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2255-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2254-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2253-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2252-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2251-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2250-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2249-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3 recall — Becton Dickinson & Company

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…

Company / brand: Becton Dickinson & Company recalls

Official ID Z-2248-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC

Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or rea…

Company / brand: Fresenius Kabi USA recalls

Official ID Z-2224-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

LVP software of the Ivenix Infusion System (IIS) recall — Fresenius Kabi USA, LLC

Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless …

Company / brand: Fresenius Kabi USA recalls

Official ID Z-2223-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Pediatric care bed recall — KAYSERBETTEN GMBH & CO. KG

If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased ris…

Company / brand: KAYSERBETTEN & CO. KG recalls

Official ID Z-2212-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Atlan A350XL recall — Draeger, Inc.

The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

Company / brand: Draeger recalls

Official ID Z-2208-2026 · Official record ↗

FDA Class I · Medical device · June 10, 2026

Atlan A350 recall — Draeger, Inc.

The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

Company / brand: Draeger recalls

Official ID Z-2207-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

ARTIS Icono biplane recall — Siemens Medical Solutions USA, Inc

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-f…

Company / brand: Siemens Medical Solutions USA recalls

Official ID Z-2206-2026 · Official record ↗

FDA Class II · Medical device · June 10, 2026

ARTIS pheno recall — Siemens Medical Solutions USA, Inc

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-f…

Company / brand: Siemens Medical Solutions USA recalls

Official ID Z-2205-2026 · Official record ↗

FDA Class II · Food · June 10, 2026