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

13151–13175 of 27721

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-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-1448-2024·2024-04-10
Medline Centurion Manual Surgical Kits Recalled for Weak Seal Risk
Medline Industries is recalling 1700 units of Centurion Manual surgical kits due to potential weak seals that could compromise sterility. The weak seal may not be detectable by users.
Product
Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP, Product Code 15MLVLCP; b) STERILE 9X12 RECLOSABLE BAG, Product Code MG912ST
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1443-2024·2024-04-10
Medline Centurion surgical kits recalled due to weak seal
Medline Industries is recalling Centurion manual surgical kits because they may have weak seals that could compromise product sterility. The defect may not be noticeable to users before the kits are used.
Product
Centurion manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10", Product Code I68905; b) VAGINAL REPAIR KIT, Product Code MNS11505; c) PTCA ADD-ON KIT, Product Code MNS11545; d) INSTRUMENT SET, Product Code SUT21355
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1451-2024·2024-04-10
Centurion umbilical cord clamp cutter recalled for potential sterility breach
Medline's Centurion umbilical cord clamp cutters may have weak seals that could compromise sterility. The defect may not be detectable during normal inspection.
Product
Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300), Product Code 67335
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-1462-2024·2024-04-10
Mobile X-ray System Structural Cable Defect Affects Safety Function
Agfa DX-D 100 mobile X-ray systems have a structural cable defect in the support column that may prevent the safety mechanism from blocking the arm if the cable fails, potentially resulting in patient injury.
Product
Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generate projection X-Ray images of human patients. Models: 5411/ 050, A5411/ 0300
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-1432-2024·2024-04-10
Laryngeal Mirror Weak Seal May Breach Sterility
Medline is recalling Centurion STERILE #5 Laryngeal Mirrors due to weak packaging seals that may not be detectable by users. The defect could result in a breach of the product's sterility if the seal fails.
Product
Centurion STERILE #5 LARYNGEAL MIRROR(505709), Product Code 67830
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1436-2024·2024-04-10
Centurion Scalpel Handles Recalled Due to Weak Seal Risk
Medline Industries is recalling Centurion scalpel handle kits due to weak seals that may compromise sterility. Users cannot always detect the defect.
Product
Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE, Product Code 66825; b) STERILE PAS #3 BLADE HANDLE (BH3PAS), Product Code I68290
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1407-2024·2024-04-10
Exactech Equinoxe Shoulder Glenoid Components Recalled for Defective Packaging
Exactech is recalling 985 shoulder implant components due to nonconforming packaging that lacks a required oxygen barrier layer. The vacuum bags do not meet packaging specifications.
Product
Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, RIGHT, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-02-32, b) 41, 44, 47, 50 head, Medium, Item Number 314-02-33, c) 44, 47, 50, 53 head, Large, Item Number 314-02-34, d) 44, 47, 50, 53 he
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1429-2024·2024-04-10
Dental Rolls Recalled for Potential Sterility Breach from Weak Seal
Centurion Sterile Cotton Dental Rolls with weak seals may have compromised sterility. Affected products may allow contamination if the seal fails.
Product
Centurion STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1418-2024·2024-04-10
Exactech Equinoxe Reverse Shoulder Liners Recalled for Packaging Nonconformance
Exactech recalls 66,646 Equinoxe Reverse Shoulder humeral liners due to nonconforming packaging lacking required oxygen barrier protection. The missing EVOH layer means units do not meet established packaging specification.
Product
Exactech Equinoxe REVERSE SHOULDER, 38mm Humeral Liner: a) +0mm, Item Number 320-38-00, b) +2.5mm, Item Number 320-38-03; Shoulder Arthroplasty
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-1426-2024·2024-04-10
Torrent Suite Dx Software versions affected by cybersecurity vulnerability
Life Technologies Corporation is recalling Torrent Suite Dx Software versions 5.14 and earlier due to a cybersecurity vulnerability that could allow unauthorized access to alter instrument settings, configurations, software, or data.
Product
Torrent Suite Dx Software versions 5.14 and earlier used in connection with Ion PGM DX Systems-IVD intended for targeted sequencing of human genomic DNA (gDNA) from peripheral whole-blood samples and DNA and RNA extracted from formalin-fixed, paraffin-embedded (FFPE) samples. The
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-1479-2024·2024-04-10
ARCHITECT Anti-HCV Reagent Kit Recalled for False Positive Results
Abbott GmbH is recalling ARCHITECT Anti-HCV Reagent Kit (7,219 units) due to falsely elevated test results when processed after certain other tests on the same instrument. The product was distributed nationwide.
Product
ARCHITECT Anti-HCV Reagent Kit, List Numbers: a) 1L79-25, b) 1L79-35
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-1405-2024·2024-04-10
Exactech Equinoxe Shoulder Components Recalled for Packaging Defect
Exactech is recalling 6,840 units of Equinoxe shoulder implant components because their vacuum packaging lacks the required oxygen barrier layer (EVOH). The defect could potentially allow material degradation during storage.
Product
Exactech Equinoxe GLENOID,KEELED, CEMENTED,47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-12, b) Medium, Item Number 314-02-13, c) Large, Item Number 314-02-14, d) Extra Large, Item Number 314-02-15, Shoulder Arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2024·2024-04-10
Centurion Surgical Hook Kits Recalled Due to Weak Seal
Medline Industries is recalling 1,520 Centurion surgical hook kits worldwide due to weak seals that may compromise sterility. The seal defect may not be detectable by users.
Product
Centurion hook kits labeled as: a) STERILE SKIN HOOK FINE (EA3975F), Product Code 66660; b) STERILE SMALL 2 PRONG SKIN HOOK (25754), Product Code 67105; c) STERILE NEWS TRACH HOOK(83300), Product Code 67810; d) STERILE LILLIE EAR HOOK DELICATE 7", Product Code I68655
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1459-2024·2024-04-10
Medline Blood Pressure Units Recalled for Manufacturing Specification Non-Compliance
Medline Industries is recalling 74,339 blood pressure units nationwide (models MDS4001, MDS4001LA, MDS4001PLUS) due to manufacturing non-compliance with specifications.
Product
Blood Pressure Unit, Model (REF) Numbers: a) MDS4001, b) MDS4001LA, c) MDS4001PLUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1110-2024·2024-04-10
Hood Country Style Cottage Cheese Recalled for Undeclared Ingredients
HP Hood is recalling Country Style Cottage Cheese 24oz due to undeclared pineapple and other ingredients. Consumers with pineapple allergies or sensitivity to listed ingredients should not consume the product.
Product
Hood Country Style Cottage Cheese 24oz (UPC 044100106385),
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0430-2024·2024-04-10
Diltiazem Hydrochloride Capsules Recalled Due to Failed Dissolution Specifications
Glenmark Pharmaceuticals is recalling 6,528 bottles of Diltiazem Hydrochloride Extended-Release Capsules nationwide because dissolution testing found the product does not meet specifications. The FDA has classified this as a Class II recall.
Product
DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1440-2024·2024-04-10
Centurion Clamp kits recalled due to potential sterility breach risk
Medline Industries is recalling Centurion Clamp kits due to potential weak seals that could compromise sterility. Affected units were distributed nationwide and internationally.
Product
Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520; b) STERILE TOWEL CLAMP, Product Code A547ST; c) ST TOWEL CLAMPS NON PERFORATING (P/S), Product Code I68080; d) STERILE TOWEL CLAMPS 5 1/2, Product Code I68085; e) STERILE TOWE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1410-2024·2024-04-10
Exactech Shoulder Implants Recalled for Improper Packaging Defect
Exactech Equinoxe glenoid shoulder implants were packaged with non-conforming bags lacking an oxygen barrier layer (EVOH), creating potential risk of material degradation. The Class II recall affects 180 units distributed nationwide and internationally.
Product
Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, LEFT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-06-22, b) 41, 44, 47, 50 head, Medium, Item Number 314-06-23, c) 44, 47, 50, 53 head, Large, Item Number 314-06-24, d) 44,
Category
Medical Device
Distribution
Distributed nationwide

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13151–13175 of 27721