Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

6151–6175 of 13666

HighFDA (Devices)·Z-2141-2024·2024-06-19
Fresenius AquaA hemodialysis water purification device pressure control malfunction
Fresenius is recalling 4 hemodialysis water purification devices for pressure control malfunctions. When concentrate pressure exceeds the 19.9 bar limit, the device stops supplying water and halts dialysis treatment.
Product
US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of water to be used for hemodialysis Vivonic Part Numbers: G02020110 Fresenius Part Number: 24-090A-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2131-2024·2024-06-19
Stimuplex A Injection Needles Recalled for DEHP Mislabeling
B Braun Medical Inc is recalling Stimuplex A injection needles because the devices are labeled as DEHP-free, but the glue used contains traces of DEHP. The recall affects 20,850 units distributed in the US and Canada.
Product
Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2034-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized At-Home Distribution
Wondfo USA has recalled Streptococcal A rapid test kits that are being sold for unauthorized at-home and direct-to-consumer use. The kits should not be used outside professional healthcare settings.
Product
Streptococcal A rapid test kits, labeled as: Wondfo Biotech Co., Ltd, WondView Strep A Test Kit, Guangzhou Wondfo Biotech Co., Ltd, Wondfo One Step Strep A Swab Test, Dealmed Medical Supplies LLC, Strep A Rapid Test Kit, Jant Pharmacal Corporation, Accustrip VALUPAK Strep A Test
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2142-2024·2024-06-19
VITROS Immunodiagnostic Calibrators Recalled for Potential Accuracy Bias
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.
Product
VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled Calibrator tube (1 per level: C1 - green, C2 - yellow, C3 - red).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2137-2024·2024-06-19
CODMAN EVD BACTISEAL Catheter Sterile Packaging Defect Recall
Integra LifeSciences recalls CODMAN EVD BACTISEAL catheters due to defects in sterile packaging that may compromise product sterility. The defect affects 106 units distributed worldwide.
Product
CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2024·2024-06-19
Aeos Robotic Digital Microscope recalled for safety mechanism failure
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Product
Aeos Robotic Digital Microscope, Product Code: PV010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2138-2024·2024-06-19
EVD Catheter Sterile Packaging Defect Recall for Intracranial Drainage
Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.
Product
CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2129-2024·2024-06-19
OMTech Desktop Laser Engraver recalled for missing safety interlocks
Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.
Product
OMTech Desktop Laser Engraver
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2031-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized Distribution
Wondfo USA has recalled 170,000 units of Clarity Strep A Rapid Test kits due to unauthorized distribution for at-home use, non-prescription use, over-the-counter use, and direct-to-consumer sales. The recall affects test kits distributed nationwide.
Product
Clarity and Clarity Diagnostics LLC, Streptococcal A rapid test kits, Labeled as: a) Clarity Strep A Rapid Test, Part Number CD-STP25, b) Clarity Diagnostics LLC, Clarity Strep A Rapid Test, Part Number CD-STP25V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2041-2024·2024-06-19
MRI Systems Power Cable Terminal Block Fire Hazard Recall
Canon Medical MRI systems are being recalled because the terminal block securing the power cable may disconnect, potentially causing electrical arcing and fire. 153 units are affected across the United States and Puerto Rico.
Product
MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504), Vantage Titan 3T MRT-3010 (MEXL-3010), Vantage Galan 3T MRT-3020 (MEXL-3020)
Category
Medical Device
Distribution
38 states
ModerateFDA (Devices)·Z-2036-2024·2024-06-19
NEOMED nonsterile pharmacy syringes recalled for missing expiration dates on labels
Avanos Medical recalls NEOMED nonsterile pharmacy syringes because expiration dates were not printed on outer shipping labels, resulting in expired products being distributed.
Product
NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Blue NonSterile, Product Code BB-S05EO; b. 12mL Oral Syringe Blue NonSterile, Product Code BB-S12EO; c. 1mL Oral Syringe Blue NonSterile, Product Code BB-S1EO; d. 2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2030-2024·2024-06-19
Strep A Rapid Test Kits Recalled for Unauthorized Distribution
Wondfo USA is recalling approximately 1.2 million Preview Strep A rapid test kits (Part Numbers PRE-STA-25 and PRE-STA-A-10) that were distributed for at-home and direct-to-consumer use. The device is intended for professional channels only.
Product
Preview Strep A, Streptococcal A rapid test kits, Part Numbers: a) PRE-STA-25, b) PRE-STA-A-10
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2132-2024·2024-06-19
Medical device nerve block needles incorrectly labeled as DEHP-free
Stimuplex A nerve block needles labeled as DEHP-free contain trace amounts of DEHP in the adhesive. B Braun is recalling approximately 1.78 million units distributed in the US and Canada.
Product
Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2032-2024·2024-06-19
Streptococcal A Rapid Test Kits Recalled for Unauthorized At-Home Distribution
Wondfo USA recalls Areta Strep A test kits (Lot E03920802) distributed for unauthorized at-home and over-the-counter use. The recall affects 75,000 units distributed nationwide.
Product
Streptococcal A rapid test kits, labeled as: Easy Healthcare Corporation, Areta Strep A Swab Test and EASY at Home Medical LLC, Areta One Step Strep A Swab Test, Part Number ARST-100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2035-2024·2024-06-19
NEOMED Pharmacy Syringes recalled due to missing expiration dates
Avanos Medical is recalling NEOMED Pharmacy Syringes because expiration dates were not printed on the outer shipping labels. Approximately 37,476 cases of various syringe sizes were distributed worldwide.
Product
NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a. 0.5mL Oral Syringe Amber NonSterile, Product Code BA-S05EO; b. 12mL Oral Syringe Amber NonSterile, Product Code BA-S12EO; c. 1mL Oral Syringe Amber NonSterile, Product Code BA-S1EO; d
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2037-2024·2024-06-19
NEOMED Oral Syringes Recalled Over Missing Expiration Dates on Labels
Avanos Medical is recalling NEOMED oral syringes because expiration dates were not printed on outer shipping labels, allowing expired units to reach customers.
Product
NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a.0.5mL Oral Syringe Orange NonSterile, Product Code BC-S05EO; b. 12mL Oral Syringe Orange NonSterile, Product Code BC-S12EO; c. 1mL Oral Syringe Orange NonSterile, Product Code BC-S1EO;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2143-2024·2024-06-19
Darby Dental Prophylaxis Paste Mislabeled with Incorrect Part Number
Young Dental Manufacturing is recalling 534 units of Darby Prophylaxis Paste with 1.23% Fluoride Ion (Lot 248607) due to incorrect part number labeling. The product was labeled as part number 045032 instead of the correct 040032.
Product
Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1920-2024·2024-06-12
Pediatric Patient Return Electrode Recalled for Reported Patient Burns
Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.
Product
MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient Return Electrode for patients weighing (0.8lb-50lb), (350g-22.7Kg), 66cm Long x 30.5cm Wide x 1.25cm. Electrosurgical use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1879-2024·2024-06-12
Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled for Device Malfunction
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
Product
Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF IAB-06850-U
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1877-2024·2024-06-12
Sevoflurane Vaporizer Component Recall Due to Hydrogen Fluoride Degradation
Getinge's sevoflurane vaporizer component may degrade into hydrogen fluoride, posing inhalation and skin exposure risks to healthcare workers and patients. The FDA Class I recall affects 120 units distributed across six U.S. states.
Product
Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
Category
Medical Device
Distribution
7 states
SevereFDA (Devices)·Z-1880-2024·2024-06-12
Arrow Ultra 8 Intra-Aortic Balloon Catheter Kit Recalled for Inflation Defect
The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.
Product
Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-05840-U
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1878-2024·2024-06-12
Intra-Aortic Balloon Catheter Kit Recalled for Inflation and Structural Defects
Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.
Product
Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2028-2024·2024-06-12
Philips Tempus LS-Manual Defibrillator may malfunction from electrical interference
Simultaneous ECG measurements with multiple devices can cause electrical interference that may prevent this defibrillator from functioning properly. The recall affects 1,745 units distributed nationwide.
Product
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1999-2024·2024-06-12
Vascular Graft Swivel Rod Separation Reported in ADVANTA VXT Devices
Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.
Product
ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2007-2024·2024-06-12
FLIXENE Vascular Graft Recall for Swivel Rod Component Separation
Atrium Medical is recalling FLIXENE vascular grafts due to complaints of separation between the Swivel Rod and Swivel Core components. The recall affects 53,308 units worldwide, including 11,236 in the US.
Product
FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

6151–6175 of 13666