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

11801–11825 of 27718

HighFDA (Devices)·Z-2326-2024·2024-07-17
Decompression Table Model E9011 Recalled for Structural Frame Defect
Pivotal Health Solutions is recalling 32 Decompression Table Model E9011 devices due to potentially insufficient rework on a lumbar frame part. The defect affects units distributed to CA, FL, TX, ID, GA, and TN.
Product
Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target treatment location, treatment pounds, and patterns of treatment.
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-2285-2024·2024-07-17
Foot-Ankle Procedure Tray Recalled for Excessive Sterilization Residue
American Contract Systems Inc is recalling 107 units of FOOT ANKLE-LF Procedure tray distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safety limits for permanent-implant devices.
Product
FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2333-2024·2024-07-17
Ophthalmic Injection Kit Recall Due to Unconfirmed Sterilization
MICROspecialties is recalling the Synergetics I Pack Injection Kit because sterilization cannot be confirmed, potentially causing post-operative wound or injection site infections. Affected units are lot P62764979R distributed in Missouri.
Product
Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060
Category
Medical Device
Distribution
1 state
HighFDA (Drugs)·D-0590-2024·2024-07-17
Bupropion Extended-Release Tablets Recalled for Dissolution Failure
Amerisource Health Services is recalling Bupropion Hydrochloride 150mg extended-release tablets nationwide due to dissolution specification failures. The tablets dissolve faster than specified limits.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2331-2024·2024-07-17
AURORA Surgiscope System Recalled for Potential Sheath Damage
Integra LifeSciences is recalling 14 units of the AURORA Surgiscope System due to potential sheath damage that could cause tissue damage or internal bleeding.
Product
AURORA Surgiscope System. Sterile, single use device that contains a Sheath, Obturator, and Imager.
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2278-2024·2024-07-17
Knee surgery procedure tray recalled for chemical contamination
American Contract Systems is recalling TOTAL KNEE procedure trays (Catalog Number BFTK01AA) due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component that exceed acceptable regulatory limits.
Product
TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2306-2024·2024-07-17
Surgical Procedure Kit Recalled for Ethylene Oxide Residual Contamination
American Contract Systems Inc is recalling the ACL PACK Surgical Procedure Kit due to elevated ethylene oxide and ethylene chlorohydrin residuals that exceed regulatory limits for permanent-contact medical devices.
Product
ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2345-2024·2024-07-17
Hemodialysis Blood Pump Rotor Spare Part Recalled for Loose Sheaves
Fresenius Medical Care is recalling hemodialysis blood pump rotor spare parts due to reports of loose or dislodged guide sheaves. The affected model is distributed nationwide in the U.S. and Canada.
Product
RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2302-2024·2024-07-17
Medical knee procedure kit recalled for excessive sterilization chemical residue
American Contract Systems Inc is recalling TOTAL KNEE-Procedure Kits due to excessive ethylene oxide and ethylene chlorohydrin residues on the cast padding component. The recall affects 85 units distributed nationwide.
Product
TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2024·2024-07-17
Knee Procedure Kit Recalled for Elevated Chemical Residuals
American Contract Systems Inc is recalling 26 TOTAL KNEE Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residues on the cast padding component that exceed safe exposure limits.
Product
TOTAL KNEE -Procedure Kit Catalog Number: QPTK95B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2024·2024-07-17
Knee Procedure Kit Recalled Due to Ethylene Oxide Residual Contamination
American Contract Systems Inc recalls 174 units of CUSTOM KNEE procedure kits due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe exposure limits for permanent contact devices.
Product
CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AG
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2024·2024-07-17
Procedure Kit Recalled for Excess Ethylene Oxide Residue in Cast Padding
American Contract Systems Inc is recalling 36 units of Hand Pack procedure kits due to ethylene oxide and ethylene chlorohydrin residuals in the cast padding component exceeding regulatory limits.
Product
HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2300-2024·2024-07-17
Hand Draping Surgical Kit Recalled for Ethylene Oxide Residue
American Contract Systems Inc is recalling the Hand Draping SJH-Procedure Kit because residual levels of ethylene oxide and ethylene chlorohydrin exceeded safe limits for permanent-contact medical devices.
Product
HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2336-2024·2024-07-17
Ophthalmic injection kit recalled due to sterilization process verification failure
MICROspecialties is recalling 804 units of the Synergetics I Pack Injection Kit due to inability to confirm proper sterilization, which could lead to post-operative wound infections or injection site infections.
Product
Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-2280-2024·2024-07-17
Arthroscopy Procedure Tray Recalled for Excess Sterilization Residue
American Contract Systems recalls the ARTHROSCOPY WOLFSON PACK BHS Procedure tray because ethylene oxide residuals on the cast padding exceeded safety limits for permanent exposure medical devices.
Product
ARTHROSCOPY WOLFSON PACK BHS Procedure tray Catalog Number: BPAR65A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0594-2024·2024-07-17
Compounded Lidocaine-Epinephrine Injectable Recalled Nationwide for Subpotent Epinephrine
Tailstorm Health Inc is recalling a compounded lidocaine-epinephrine injection nationwide due to subpotent epinephrine component. The recall affects 12,525 vials of lot number 2311003.
Product
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2329-2024·2024-07-17
Cardiovascular Procedure Kits Recalled for Potential Syringe Design Defects
Cardinal Health recalls 17,445 cardiovascular procedure kits nationwide containing potentially defective syringes that could cause inaccurate dosing or device leakage.
Product
Presource kits and trays, labeled as: 1) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC3; 2) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC4; 3) Cardiovascular Procedure Kit, Catalog Number SAN29ANCCL; 4) Cardiovascular Procedure Kit, Catalog Number SAN29ANCC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2024·2024-07-17
Endoscopic Vessel Harvesting System Recalled for C-Ring Wire Straightening
Maquet Cardiovascular recalled 2,463 VASOVIEW HEMOPRO 2 surgical systems due to C-Ring wire straightening and component misalignment affecting tool positioning. No injuries have been reported.
Product
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2310-2024·2024-07-17
Hand Procedure Kit Recalled for Excess Ethylene Oxide Residuals
American Contract Systems recalls HAND PACK-Procedure Kits due to excess ethylene oxide and ethylene chlorohydrin residuals on the cast padding component, exceeding safe permanent-contact exposure limits.
Product
HAND PACK-Procedure Kit Catalog Number: WEHD16B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2024·2024-07-17
Dental abutment recall due to incorrect product packaging and labeling
Preat Corp recalled 7 units of 9006767 Astra EV 4.8mm Milled Titanium Abutments due to incorrect products being packaged and labeled. Affected units were distributed in California, Missouri, and Nevada.
Product
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-2303-2024·2024-07-17
Arthroscopy Kit Recalled for Excessive Sterilant Residue on Padding
American Contract Systems is recalling 27 arthroscopy procedure kits because the cast padding component contains ethylene oxide and ethylene chlorohydrin residues exceeding safe limits for permanent exposure devices.
Product
ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2024·2024-07-17
Arthroscopy Procedure Kit Recalled Due to Ethylene Oxide Residue
American Contract Systems Inc is recalling 27 arthroscopy procedure kits because ethylene oxide and ethylene chlorohydrin residuals in the cast padding exceeded safe exposure limits for permanent implants.
Product
ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2024·2024-07-17
Knee Arthroscopy Procedure Kit Recalled for Sterilization Chemical Residue
American Contract Systems Inc is recalling 36 units of its knee arthroscopy procedure kit due to excessive sterilization chemical residues in the cast padding component that exceed safe exposure limits.
Product
KNEE ARTHROSCOPY-Procedure Kit Catalog Number: QPKA35A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2291-2024·2024-07-17
Knee Arthroscopy Pack Recalled for Excess Sterilization Residues
American Contract Systems Inc. is recalling 84 knee arthroscopy packs (Catalog Number MEKA12R) distributed nationwide due to ethylene oxide and ethylene chlorohydrin residuals exceeding safe limits for permanent exposure medical devices.
Product
KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2274-2024·2024-07-17
Arthroscopy Pack Recalled for Excessive Sterilization Chemical Residue
American Contract Systems is recalling 345 units of the AHAR50K Standard Arthroscopy Pack due to ethylene oxide residue levels exceeding regulatory limits. Affected lot numbers are 638231, 962241, and 898241.
Product
AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K
Category
Medical Device
Distribution
Distributed nationwide

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11801–11825 of 27718