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

5726–5750 of 27364

HighFDA (Devices)·Z-1514-2024·2024-04-17
PEG Feeding Tube Kit Recalled for Blocked Lumen Preventing Guidewire Advancement
Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.
Product
EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509051
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1508-2024·2024-04-17
Nucleic Acid Isolation Device Recall: EZ2 Connect MDx-IVD Heater Failure
Qiagen Sciences is recalling 168 units of the EZ2 Connect MDx-IVD nucleic acid isolation device due to insufficient welding that causes heater cable embrittlement and device malfunction, resulting in sample loss during testing.
Product
EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model Number: 9003230
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2024·2024-04-17
EndoVive 20Fr Push Safety PEG Kit Recall Due to Blocked Lumen Risk
Boston Scientific is recalling the EndoVive 20Fr PEG feeding kit due to blockage in the barb connector that can prevent proper placement. The blockage may lead to prolonged procedures, bleeding, gastric leakage, and aspiration risk.
Product
EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509011
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1351-2024·2024-04-10
Mojo Full Face CPAP Mask Recall: Magnet Safety Update
SleepNet Corporation is recalling 23,042 Mojo Full Face CPAP masks worldwide because the masks contain magnets that require updated contraindications and warning language.
Product
Mojo Full Face with Headgear, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1354-2024·2024-04-10
Mojo 2 Full Face Non Vented Mask Recalled for Magnet Safety Concerns
SleepNet Corporation is recalling Mojo 2 Full Face Non Vented Masks due to magnets in the device and updated contraindications and warnings. The recall affects 2,107 units distributed worldwide.
Product
Mojo 2 Full Face Non Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1353-2024·2024-04-10
Mojo 2 Full Face Vented Mask Recalled: Magnet Contraindications Updated
SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.
Product
Mojo 2 Full Face Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1356-2024·2024-04-10
iQ 2 Nasal Vented Mask Recalled for Magnet Safety Warnings
SleepNet Corporation is recalling the iQ 2 Nasal Vented Mask due to magnets requiring updated contraindication and warning language. Approximately 2,477 units distributed worldwide are affected.
Product
iQ 2 Nasal Vented Mask
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1352-2024·2024-04-10
Mojo Non Vented Full Face Mask warning updated for magnet hazard
SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.
Product
Mojo Non Vented Full Face Mask with Headgear, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1355-2024·2024-04-10
Mojo 2 CPAP Masks Recalled Worldwide for Magnet Safety Contraindication Update
SleepNet Corporation is recalling Mojo 2 Full Face CPAP masks (1,268 units worldwide) to update contraindications and warning language due to magnets in the masks. The FDA classified this as a Class I recall.
Product
Mojo 2 Full Face AAV Non Vented Mask, All Sizes
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1357-2024·2024-04-10
Phantom 2 Nasal Vented Mask recalled due to magnetic device interference risk
SleepNet is recalling the Phantom 2 Nasal Vented Mask to update contraindications and warning information related to magnets in the device. The recall affects 2,417 units distributed worldwide.
Product
Phantom 2 Nasal Vented Mask
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1406-2024·2024-04-10
Exactech shoulder implant components recalled for nonconforming packaging
Exactech is recalling 805 Equinoxe glenoid implant components due to nonconforming vacuum packaging that lacks required oxygen barrier protection, which could affect sterility.
Product
Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, LEFT, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-02-22, b) 41, 44, 47, 50 head, Medium, Item Number 314-02-23, c) 44, 47, 50, 53 head, Large, Item Number 314-02-24, d) 44, 47, 50, 53 hea
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1430-2024·2024-04-10
Sterile blood collection tubes recalled for weak seal defect
MEDLINE INDUSTRIES is recalling Centurion 10mL sterile blood collection tubes due to weak seals that may compromise sterility and allow contamination if they fail.
Product
Centurion STERILE BLOOD COLLECTION TUBE,10ML, Product Code 6430ST
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1465-2024·2024-04-10
Covidien Auto Suture Trocar Recalled for Potential Seal Disengagement
Covidien is recalling approximately 124,863 Auto Suture Structural Balloon Trocars worldwide due to potential seal disengagement when used incorrectly with mesh products.
Product
Covidien Auto Suture" Structural Balloon Trocar, Product Number OMS-T10SB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2024·2024-04-10
Abbott ARCHITECT STAT Myoglobin Reagent Kit recalled due to manufacturing defect
Abbott is recalling certain myoglobin test kits because of manufacturing defects that could lead to incorrect results and delayed heart attack diagnosis.
Product
ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2024·2024-04-10
Centurion PICC Line Securement Kit Recalled for Weak Seal
MEDLINE is recalling the Centurion PICC Line Securement Kit because its seal may be weak, potentially allowing sterility breach. Users may not be able to detect the weakness.
Product
Centurion PICC LINE SECUREMENT KIT, Product Code IVS565
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2024·2024-04-10
Karl Storz Grasping Forceps Recalled for Inadequate Reprocessing Validation
FDA recalls 190 units of Karl Storz grasping forceps due to inadequate evidence validating safe reprocessing and sterilization of the instruments.
Product
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2024·2024-04-10
Stryker Infinity Resection Adjustment Block Recall: Missing Locking Screw
Stryker recalled specific lots of Infinity Resection Adjustment Blocks due to a missing internal screw that locks the medial/lateral adjustment mechanism. The defect affects 47 units used in ankle arthroplasty procedures.
Product
stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1416-2024·2024-04-10
Exactech Equinoxe Reverse Shoulder Humeral Liners Recalled for Packaging Defect
Exactech humeral liners used in shoulder replacement are recalled because the vacuum packaging lacks a required oxygen barrier layer (EVOH), violating established packaging specifications.
Product
Exactech Equinoxe REVERSE SHOULDER,36mm Humeral Liner: a) +0mm, Item Number 320-36-00, b) +2.5mm, Item Number 320-36-03; Shoulder Arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1460-2024·2024-04-10
Trumpet Needle Guide Ring May Detach Under Excessive Pressure
Technicality Inc. is recalling Trumpet Needle Guides (Cat# TMS-200) because the ring can detach when excessive pressure is applied. Approximately 20,000 units distributed nationwide in Illinois are affected.
Product
Trumpet, Needle Guide, Cat# TMS-200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1438-2024·2024-04-10
Centurion Hemostat Kits Recalled Due to Weak Seal Sterility Breach Risk
Medline Industries is recalling Centurion Hemostat kits because weak seals may allow sterile contents to become contaminated. The weak seal may not be apparent to users before the instrument is used.
Product
Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEMOSTAT (MHS103), Product Code 66145; c) STERILE STRT KELLY HEMOSTAT (SK8039), Product Code 66170; d) STERILE CURV KELLY HEMOSTAT (CK8040), Product Code 66175
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1398-2024·2024-04-10
BD Phoenix diagnostic panel recalled for drug cross-contamination
Becton Dickinson recalls BD Phoenix NMIC-306 microbiology diagnostic panels due to confirmed drug cross-contamination that may lead to incorrect bacterial identification and delayed treatment.
Product
BD Phoenix NMIC-306 Panel is a self-inoculating (when used with a BD Phoenix Automated Microbiology System) polystyrene panel (tray) containing control wells and substrate wells with dried biochemical substrates that use traditional qualitative microbiology methods such as fermen
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1468-2024·2024-04-10
Covidien Auto Suture Trocar Recall: Potential Seal Disengagement With Incorrect Mesh Use
Covidien is recalling 93,673 Auto Suture Blunt Tip Trocars due to potential seal disengagement when mesh products are used incorrectly. Improper use could compromise device integrity during laparoscopic procedures.
Product
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1445-2024·2024-04-10
Suture Removal and Staple Remover Kits Recalled for Weak Seal
Medline Industries is recalling suture removal trays and staple remover kits due to weak seals that may compromise product sterility. Approximately 23,290 units were distributed in the US, Panama, and Canada.
Product
Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code TRI55405; b) SUTURE REMOVAL SET, Product Code 60265 MEDLINE manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code 60280; b) SUTURE REMOVAL TRAY, Product Code 86125; c) SUT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2024·2024-04-10
Medline Centurion Surgical Retractors Recalled for Potential Sterility Breach
Medline is recalling Centurion surgical retractor kits (760 units) due to a weak seal that could compromise sterility if it fails. The weakness may not be detectable by users.
Product
Centurion retractor kits labeled as: a) STERILE 6-1/2" SENN RETRACTOR (ST7185), Product Code 66795; b) STERILE RAGNELL RETRACTOR (RR602), Product Code 67525; c) ST. SENN RETRACTOR 3 PRG BLUNT (ST7085), Product Code 37535
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1452-2024·2024-04-10
Sterile tape/pen pack recalled for potential sterility breach
Medline M1S0179 sterile tape/pen packs may have weak seals that could compromise product sterility. The weakness may not be visible during normal inspection.
Product
MEDLINE M1S0179 STRL TAPE/PEN PACK, Product Code P519582A
Category
Medical Device
Distribution
Distributed nationwide

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5726–5750 of 27364