Latest recalls — page 9
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 801–900, newest first.
FDA Class II · Drug · September 9, 2026
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
Company / brand: Allies Group recalls
Official ID D-0824-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.
Company / brand: Allies Group recalls
Official ID D-0823-2026 ·
Official record ↗
FDA Class III · Drug · September 9, 2026
Presence of Foreign Tablets/Capsules
Company / brand: Bionpharma recalls
Official ID D-0822-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0821-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0820-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0819-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0818-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0817-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0816-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0815-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0814-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0813-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0812-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0811-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0810-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0809-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0808-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0807-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0806-2026 ·
Official record ↗
FDA Class II · Drug · September 9, 2026
CGMP Deviations
Company / brand: Baxter Healthcare recalls
Official ID D-0805-2026 ·
Official record ↗
NHTSA · Vehicle · September 7, 2026
An inoperative instrument cluster will fail to display critical safety information, such as vehicle speed and warning lights, increasing the risk of a crash.
Company / brand: Bombardier Recreational Products recalls
Official ID 26V575000 ·
Official record ↗
NHTSA · Vehicle · September 5, 2026
An overheated printed circuit board increases the risk of a fire.
Company / brand: Kibbi recalls
Official ID 26V574000 ·
Official record ↗
NHTSA · Vehicle · September 3, 2026
An unexpected engine shut down can increase the risk of a crash. Additionally, transferring passengers from the disabled bus can increase the risk of injury.
Company / brand: Nova Bus recalls
Official ID 26V573000 ·
Official record ↗
NHTSA · Vehicle equipment · September 3, 2026
An unexpected engine shut down can increase the risk of a crash. Additionally, transferring passengers from the disabled bus can increase the risk of injury.
Company / brand: Nova Bus recalls
Official ID 26E062000 ·
Official record ↗
CPSC · Bicycles & Accessories · September 3, 2026
The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard.
Company / brand: MONDRAKER USA recalls
Official ID 26746 ·
Official notice ↗
CPSC · Cleaners/Cleaning Products · September 3, 2026
The recalled products may contain bacteria, including Pseudomonas aeruginosa, which is an environmental organism found widely in soil and water. People with weakened immune systems…
Company / brand: Clorox Manufacturing Company of Puerto Rico recalls
Official ID 26741 ·
Official notice ↗
CPSC · Adapter/Power Supply/Charger/Battery · September 3, 2026
The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
Company / brand: Truststone Group of New York recalls
Official ID 26740 ·
Official notice ↗
CPSC · Toys · September 3, 2026
The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard.
Company / brand: The William Carter Company recalls
Official ID 26739 ·
Official notice ↗
CPSC · Squeeze Or Squeaker Toys · September 3, 2026
The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a child’s body, resulting in…
Company / brand: Xiamen Liuhui Electric Technology Co recalls
Official ID 26738 ·
Official notice ↗
CPSC · Squeeze Or Squeaker Toys · September 3, 2026
The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If …
Company / brand: OKK Trading recalls
Official ID 26737 ·
Official notice ↗
CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026
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: Airiva recalls
Official ID 26736 ·
Official notice ↗
CPSC · Chairs, Not Specified · September 3, 2026
The backrests of the chairs can detach, posing a fall hazard to consumers.
Company / brand: Bureau Office recalls
Official ID 26735 ·
Official notice ↗
CPSC · Air Conditioners · September 3, 2026
The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard.
Company / brand: Daikin Comfort Technologies Manufacturing recalls
Official ID 26734 ·
Official notice ↗
CPSC · Adult Bed Rails · September 3, 2026
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: Fangzhou Overseas Consulting Shenzhen Co recalls
Official ID 26733 ·
Official notice ↗
CPSC · Toys & Children · September 3, 2026
The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.
Company / brand: SHEIN Distribution of Los Angeles recalls
Official ID 26732 ·
Official notice ↗
CPSC · Speakers · September 3, 2026
The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard.
Company / brand: Audio Partnership recalls
Official ID 26731 ·
Official notice ↗
CPSC · Desks, Dressers, Chests, Bureaus, Or Buffets · September 3, 2026
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: Nanjing Wu Hai Smart Home Appliance Store recalls
Official ID 26730 ·
Official notice ↗
NHTSA · Vehicle · September 2, 2026
A vehicle with an incorrect maximum capacity weight value may be overloaded, increasing the risk of a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V571000 ·
Official record ↗
NHTSA · Vehicle · September 2, 2026
An unexpected loss of drive power increases the risk of a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V570000 ·
Official record ↗
FDA Not Yet Classified · Drug · September 2, 2026
Cross Contamination with Other Products
Company / brand: Safecor Health recalls
Official ID EVT-99666-wagogx ·
Official record ↗
FDA Not Yet Classified · Food · September 2, 2026
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
Company / brand: Africando Foods recalls
Official ID EVT-99642-1ffccqp ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-3039-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-3038-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-3037-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and…
Company / brand: GE Medical Systems Information Technologies recalls
Official ID Z-3036-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
Company / brand: Olympus of the Americas recalls
Official ID Z-3035-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This…
Company / brand: IMRIS Imaging recalls
Official ID Z-3034-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This…
Company / brand: IMRIS Imaging recalls
Official ID Z-3033-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Company / brand: Healthmark Industries Co recalls
Official ID Z-3032-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Company / brand: Healthmark Industries Co recalls
Official ID Z-3031-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may cause the ruler measurement to be inaccurate.
Company / brand: FUJIFILM Healthcare Americas recalls
Official ID Z-3030-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3029-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3028-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3027-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3026-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3025-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3024-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3023-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3022-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3021-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3020-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Kits contain a potentially contaminated component which were recalled by the manufacturer
Company / brand: Medline Industries recalls
Official ID Z-3019-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
Company / brand: ConMed recalls
Official ID Z-3018-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis m…
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3017-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Company / brand: Henry Schein recalls
Official ID Z-3016-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Company / brand: Henry Schein recalls
Official ID Z-3015-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.
Company / brand: Canon Medical System recalls
Official ID Z-3014-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Company / brand: Midmark recalls
Official ID Z-3013-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Company / brand: Midmark recalls
Official ID Z-3012-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3011-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3010-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3009-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3008-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3007-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3006-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Company / brand: AVID Medical recalls
Official ID Z-3005-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Software issue may cause measurements to be displayed inaccurately.
Company / brand: Merge Healthcare recalls
Official ID Z-3004-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Company / brand: American Contract Systems recalls
Official ID Z-3003-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Company / brand: American Contract Systems recalls
Official ID Z-3002-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Company / brand: American Contract Systems recalls
Official ID Z-3001-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representativ…
Company / brand: American Contract Systems recalls
Official ID Z-3000-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Component labeling discrepancy
Company / brand: Medline Industries recalls
Official ID Z-2999-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary…
Company / brand: Hollister Ulc recalls
Official ID Z-2998-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…
Company / brand: Medline Industries recalls
Official ID Z-2997-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…
Company / brand: Medline Industries recalls
Official ID Z-2996-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…
Company / brand: Medline Industries recalls
Official ID Z-2995-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification lev…
Company / brand: Medline Industries recalls
Official ID Z-2994-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…
Company / brand: Medline Industries recalls
Official ID Z-2993-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…
Company / brand: Medline Industries recalls
Official ID Z-2992-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,…
Company / brand: Medline Industries recalls
Official ID Z-2991-2026 ·
Official record ↗
FDA Class II · Medical device · September 2, 2026
Potential of failing to trigger clinical scan during Bolus Tracking.
Company / brand: Philips Healthcare (Suzhou) Co recalls
Official ID Z-2988-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
Company / brand: Africando Foods recalls
Official ID H-1381-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Product has the potential to be spoiled.
Company / brand: Horizon Organic Dairy recalls
Official ID H-1333-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Product may have been improperly pasteurized.
Company / brand: UPSTATE NIAGARA COOPERATIVE recalls
Official ID H-1332-2026 ·
Official record ↗
FDA Class I · Food · September 2, 2026
Undeclared Egg Allergen
Company / brand: Jaime's Foods ATX recalls
Official ID H-1301-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Label does not declare walnuts in English
Company / brand: Byron White Formulas recalls
Official ID H-1278-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Label does not declare walnuts in English
Company / brand: Byron White Formulas recalls
Official ID H-1277-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
Label does not declare walnuts in English
Company / brand: Byron White Formulas recalls
Official ID H-1276-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coco…
Company / brand: Lidl US TRADING recalls
Official ID H-1275-2026 ·
Official record ↗
FDA Class II · Food · September 2, 2026
The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coco…
Company / brand: Lidl US TRADING recalls
Official ID H-1274-2026 ·
Official record ↗
Official sources
Government sources last checked October 22, 2026 at 12:00 PM UTC.