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

6201–6225 of 40007

HighFDA (Devices)·Z-2772-2024·2024-09-04
Medline Centurion Procedure Kits Recalled for Syringe Quality Issues
Medline is recalling Centurion procedure kits because they contain plastic syringes affected by a March 2024 FDA Safety Alert regarding leaks and breakage.
Product
Centurion procedure kits, labeled as: 1) ARTHROGRAM TRAY, Pack Number DYNDH1349; 2) ARTHROGRAM TRAY-LF, Pack Number SPEC0400; 3) ARTHROGRAM/LP/MYELOGRAM TRAY, Pack Number PT220; 4) BIOPSY KIT, Pack Number DYNDH1570; 5) BIOPSY TRAY-LF, Pack Number SPEC4380; 6) BMA BX
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2763-2024·2024-09-04
Medline Recalls LEEP and Trab Buckle Kits Due to Syringe Defects
Medline is recalling specific LEEP and Trab Buckle procedural kits because they contain plastic syringes with leaks or breakage risks.
Product
Medline procedural kits labeled as: 1) LEEP PACK, Pack Number DYNJ40348G; 2) TRAB BUCKLE DSC, Pack Number DYNJ63036B
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2858-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Defect
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001315;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2918-2024·2024-09-04
CustomEyes Procedure Packs with Sol-M Syringes Recalled by Beaver Visitec International
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs (Lot 6066752) containing Sol-M syringes. Approximately 22 units distributed nationwide in the US have been affected.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001836;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2812-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Defect
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000508;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2828-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling 59 BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000828;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2873-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001478;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2905-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M syringes recalled
Beaver Visitec International is voluntarily recalling 82 units of CustomEyes Procedure Packs containing Sol-M syringes due to a manufacturer recall. Affected lot numbers 6070885 and 6074819.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001711;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2866-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Syringe Component Issue
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The voluntary recall affects 196 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001382;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2906-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M syringes recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-Millennium Medical (Sol-M) syringes, affecting 126 units distributed nationwide. The recall was initiated following a manufacturer recall of the syringe components.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001712;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2863-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M syringes recalled
BVI CustomEyes Procedure Packs containing Sol-Millennium Medical syringes are being voluntarily recalled by the FDA. The affected 1ml Luer Lock and Luer Slip syringes were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001375;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2832-2024·2024-09-04
Voluntary Recall of BVI CustomEyes Procedure Packs With Sol-M Syringes
BVI voluntarily recalls CustomEyes Procedure Packs because they contain syringes recalled by their manufacturer, Sol-Millennium Medical, Inc. Approximately 94 units were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000910;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2925-2024·2024-09-04
BVI CustomEyes Procedure Packs recalled due to incorrect syringes
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs because they contain syringes manufactured by Sol-Millennium Medical instead of the intended product. The recall involves 57 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001933;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2893-2024·2024-09-04
BVI CustomEyes Procedure Packs Containing Sol-M Syringes Recalled Nationwide
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs that contain Sol-M syringes due to a voluntary recall by the syringe manufacturer. The recall affects 170 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001629;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2928-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Defective Sol-M Syringes
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall by their manufacturer. Approximately 332 units were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001944;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2937-2024·2024-09-04
FDA Recalls BVI CustomEyes Procedure Packs Containing Sol-M Syringes
Beaver Visitec International has voluntarily recalled 56 units of BVI CustomEyes Procedure Packs containing Sol-Millennium Medical syringes. The recall involves low dead space and luer slip tip syringes distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002075;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2834-2024·2024-09-04
BVI CustomEyes Procedure Packs containing Sol-M syringes recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing defective Sol-M syringes. The voluntary recall affects products distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000960;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2816-2024·2024-09-04
BVI CustomEyes Procedure Packs containing Sol-M syringes recalled nationwide
Procedure packs containing Sol-M manufactured syringes are being voluntarily recalled nationwide. The affected product is part number 58000603.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000603;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2912-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Components
Beaver Visitec recalls BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes subject to manufacturing defect concerns. 17 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001774;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2901-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Defective Syringes
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs that contain Sol-M syringes due to a manufacturer's voluntary recall. The nationwide recall affects Luer Lock and Luer Slip 1ml syringes in the procedure packs.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001693;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2932-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes are being recalled in a voluntary action. 207 units with Part Number 58001999 are distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001999;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2789-2024·2024-09-04
BVI CustomEyes Procedure Packs containing syringes recalled nationwide
BVI CustomEyes Procedure Packs containing Sol-M syringes are subject to a voluntary recall affecting 73 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584712;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2840-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Sol-M Syringe Issue
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical, which are subject to a separate voluntary recall.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001048;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2831-2024·2024-09-04
Voluntary Recall of BVI CustomEyes Procedure Packs with Sol-M Syringes
Beaver Visitec International is voluntarily recalling 1,429 units of BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The packs were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000873;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2911-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Nationwide for Syringe Defects
Beaver Visitec International has recalled 115 units of BVI CustomEyes Procedure Packs containing Sol-M syringes distributed nationwide. The voluntary recall addresses a manufacturing issue with the syringes included in the procedure packs.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001764;
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

6201–6225 of 40007