Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1–100, newest first.
A ball joint that separates from the lower control arm can cause a loss of vehicle control, increasing the risk of a crash.
Company / brand: Subaru recalls
Official ID 26V685000 · Official record ↗
An unsecured refrigerator may move or tip over during transit, increases the risk of injury.
Company / brand: Forest River recalls
Official ID 26V684000 · Official record ↗
Wheel detachment can result in a loss of vehicle control, increasing the risk of a crash.
Company / brand: Porsche Cars North America recalls
Official ID 26V682000 · Official record ↗
A unprotected slide switch can cause the wire to overheat, increasing the risk of a fire.
Company / brand: Forest River recalls
Official ID 26V681000 · Official record ↗
In the event of a short circuit, inadequate protection increases the risk of a fire.
Company / brand: Alliance RV recalls
Official ID 26V680000 · Official record ↗
Disengagement of the driveline may cause a loss of power to the rear drive axle, increasing the risk of a crash.
Company / brand: Spartan Fire recalls
Official ID 26V676000 · Official record ↗
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail …
Company / brand: Opal Vista recalls
Official ID 27029 · Official notice ↗
The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through ingestion, and certa…
Company / brand: Primark US recalls
Official ID 27028 · Official notice ↗
The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby to become entrapped be…
Company / brand: Papablic recalls
Official ID 27027 · Official notice ↗
Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards.
Company / brand: Loving Thyself Rocks recalls
Official ID 27026 · Official notice ↗
The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard.
Company / brand: HatsanUSA recalls
Official ID 27025 · Official notice ↗
The recalled thermal laminators can overheat, posing a fire hazard.
Company / brand: 3M Company recalls
Official ID 27024 · Official notice ↗
A bunk restraint with improperly secured webbing may fail to adequately restrain vehicle occupants during a crash, increasing the risk of injury.
Company / brand: Paccar Incorporated recalls
Official ID 26V674000 · Official record ↗
A fuel leak in the presence of an ignition source can increase the risk of a fire.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V673000 · Official record ↗
Loss of steering control increases the risk of a crash or injury.
Company / brand: KTM North America recalls
Official ID 26E071000 · Official record ↗
Potential contamination due to E. coli O26:H11.
Company / brand: Sierra Nevada Cheese Company recalls
Official ID EVT-99986-1nddy38 · Official record ↗
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Company / brand: Centric Compounding recalls
Official ID EVT-99860-15i85aw · Official record ↗
A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an…
Company / brand: Intellijoint Surgical recalls
Official ID Z-0119-2027 · Official record ↗
A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a docum…
Company / brand: Steris recalls
Official ID Z-0118-2027 · Official record ↗
Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
Company / brand: LeMaitre Vascular recalls
Official ID Z-0117-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0116-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0115-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0114-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0113-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0112-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0111-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0110-2027 · Official record ↗
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Company / brand: Mindray DS USA recalls
Official ID Z-0109-2027 · Official record ↗
Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motio…
Company / brand: Canon Medical System recalls
Official ID Z-0108-2027 · Official record ↗
During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be fo…
Company / brand: POLYMEDCO recalls
Official ID Z-0107-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0106-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0105-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0104-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0103-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0102-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0101-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0100-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0099-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0098-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0097-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0096-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0095-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0094-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0093-2027 · Official record ↗
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Company / brand: AVID Medical recalls
Official ID Z-0092-2027 · Official record ↗
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
Company / brand: Onkos Surgical recalls
Official ID Z-0091-2027 · Official record ↗
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
Company / brand: Onkos Surgical recalls
Official ID Z-0090-2027 · Official record ↗
Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds…
Company / brand: Nihon Kohden America recalls
Official ID Z-0089-2027 · Official record ↗
Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed verification test results in o…
Company / brand: Medtronic MiniMed recalls
Official ID Z-0088-2027 · Official record ↗
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the fr…
Company / brand: Medline Industries recalls
Official ID Z-0087-2027 · Official record ↗
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the fr…
Company / brand: Medline Industries recalls
Official ID Z-0086-2027 · Official record ↗
Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to particulate embolization,…
Company / brand: Stryker Sustainability Solutions recalls
Official ID Z-0085-2027 · Official record ↗
Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to us…
Company / brand: Beckman Coulter recalls
Official ID Z-0084-2027 · Official record ↗
Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use …
Company / brand: Beckman Coulter recalls
Official ID Z-0083-2027 · Official record ↗
Potential for false negative patient results.
Company / brand: DRG International recalls
Official ID Z-0082-2027 · Official record ↗
Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and irrigation, formation of s…
Company / brand: Safeguard US Operating recalls
Official ID Z-0081-2027 · Official record ↗
Lack of 510(k) clearance.
Company / brand: Limitless Cryo Spa recalls
Official ID Z-0080-2027 · Official record ↗
Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the pati…
Company / brand: Cardinal Health 200 recalls
Official ID Z-0079-2027 · Official record ↗
Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended system motion.
Company / brand: PHILIPS MEDICAL SYSTEMS recalls
Official ID Z-0078-2027 · Official record ↗
Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
Company / brand: GRI Medical & Electronic Technology Co recalls
Official ID Z-0077-2027 · Official record ↗
Due to a manufacturing issue (inadequate weld) for patient head positioning system.
Company / brand: QUANTUM OPS recalls
Official ID Z-0076-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0075-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0074-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0073-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0072-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0071-2027 · Official record ↗
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential…
Company / brand: Steris recalls
Official ID Z-0070-2027 · Official record ↗
An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
Company / brand: Medical Action Industries recalls
Official ID Z-0069-2027 · Official record ↗
Egg was not declared in the Contains statement.
Company / brand: J K Patisserie & Bakery recalls
Official ID H-0027-2027 · Official record ↗
Soy was not declared in the Contains statement.
Company / brand: J K Patisserie & Bakery recalls
Official ID H-0026-2027 · Official record ↗
Product contains undeclared soybean oil and soy lecithin in the Ingredient Statement. Soy was not declared in the Contains statement.
Company / brand: J K Patisserie & Bakery recalls
Official ID H-0025-2027 · Official record ↗
Undeclared soy allergen: soybean oil and soy lecithin
Company / brand: Saint Francis Apizza recalls
Official ID H-0024-2027 · Official record ↗
Undeclared soy allergen: soybean oil and soy lecithin
Company / brand: Saint Francis Apizza recalls
Official ID H-0023-2027 · Official record ↗
Undeclared soy allergen: soybean oil and soy lecithin
Company / brand: Saint Francis Apizza recalls
Official ID H-0022-2027 · Official record ↗
Undeclared soy allergen: soybean oil and soy lecithin
Company / brand: Saint Francis Apizza recalls
Official ID H-0021-2027 · Official record ↗
Staphylococcus aureus detected in product.
Company / brand: SWEET SENSI recalls
Official ID H-0020-2027 · Official record ↗
Product contains undeclared Sildenafil and Tadalafil.
Company / brand: A&P CREATIONS recalls
Official ID H-0017-2027 · Official record ↗
Product contains undeclared Sildenafil and Tadalafil.
Company / brand: A&P CREATIONS recalls
Official ID H-0016-2027 · Official record ↗
Undeclared milk, cheese declared
Company / brand: QUESO PALMITA GP recalls
Official ID H-0015-2027 · Official record ↗
Contamination with Listeria monocytogenes
Company / brand: GIAS FOOD recalls
Official ID H-0014-2027 · Official record ↗
Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination.
Company / brand: Berlin Seeds recalls
Official ID H-0013-2027 · Official record ↗
The chicken salad sandwich has an improperly declared allergen (egg). While egg is included in the ingredients list on the package label, it is not included in the allergen Contain…
Company / brand: FRESHPOINT CENTRAL FLORIDA recalls
Official ID H-0012-2027 · Official record ↗
Undeclared Milk.
Company / brand: The Better Bakehouse Snack Company recalls
Official ID H-0011-2027 · Official record ↗
Undeclared Yellow No. 6 and/or Yellow No. 5
Company / brand: Pepsico recalls
Official ID H-0009-2027 · Official record ↗
Bean Dip Trays contains recalled Peperoncini (pepper) which was recalled due to pest issue.
Company / brand: WinCo Foods recalls
Official ID H-0008-2027 · Official record ↗
Potential contamination with foreign objects: mice.
Company / brand: G L Mezzetta recalls
Official ID H-0007-2027 · Official record ↗
Seeds may have been contaminated with E.coli
Company / brand: LEASA Industries Co recalls
Official ID H-0003-2027 · Official record ↗
Seeds may have been contaminated with E. coli
Company / brand: LEASA Industries Co recalls
Official ID H-0002-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Apothecary Pharma recalls
Official ID D-0037-2027 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Apothecary Pharma recalls
Official ID D-0036-2027 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0035-2027 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0034-2027 · Official record ↗
Failed Impurities/Degradation Specifications
Company / brand: SUN PHARMACEUTICAL INDUSTRIES recalls
Official ID D-0033-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0032-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0031-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0030-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0029-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0028-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0027-2027 · Official record ↗
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Company / brand: Carolina Infusion recalls
Official ID D-0026-2027 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.