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

13101–13125 of 27722

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 (Food)·F-1129-2024·2024-04-17
Whitley's Peanut Factory Deluxe Nut Mix recalled for undeclared allergens
Whitley Peanut Factory is recalling Deluxe Nut Mix due to undeclared allergens (peanuts, milk, soy, wheat, and sesame) not listed on the product label. Consumers with allergies should not consume this product.
Product
Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case boxes.
Category
Food
Distribution
28 states
HighFDA (Food)·F-1122-2024·2024-04-17
Ground cinnamon bulk product recalled due to elevated lead levels
Tasty-Sawa ground cinnamon in 55.11-pound bags distributed in Florida, Georgia, North Carolina, Trinidad and Tobago, and Guyana is being recalled due to elevated lead levels. Consumers should stop using this product immediately.
Product
Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Origin Vietnam
Category
Food
Distribution
3 states
HighFDA (Food)·F-1144-2024·2024-04-17
Squash casserole recalled for missing ingredient and allergen labeling
Robeson Enterprises is recalling its Pies & Sides squash casserole due to missing ingredient list labeling. The product contains undisclosed allergens (milk, eggs, soy, fish, wheat).
Product
PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FISH, WHEAT PIES & SIDES MOUNT HOLLY, NC
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1486-2024·2024-04-17
Patient lift hanger bar may come loose, posing fall risks
Certain patient lift models may have a hanger bar that could come loose during use, potentially causing patient falls. Approximately 10 units distributed to TX, IL, OK, and CA are affected.
Product
Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1487-2024·2024-04-17
Medline Adult Portable Bed Rails Recalled for Safety Standard Failures
Medline is recalling certain lots of adult portable bed rails that were manufactured after the mandatory compliance date but failed to meet required safety standards, potentially posing a fall risk.
Product
Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1132-2024·2024-04-17
Egg Salad Sandwich Recalled for Undeclared Fish Allergen Mislabeling
Tuna salad sandwiches were mislabeled as egg salad, creating an undeclared fish allergen risk for consumers. The recall affects 551 units distributed to institutions and retailers across ten states.
Product
Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-1482-2024·2024-04-17
RayStation Software Use Error Could Cause Incorrect Radiation Dose Calculations
RayStation radiation therapy planning software versions 8B through 2024A contain a use error that can incorrectly select silicon material for silicone gel polymer implant dose calculations, potentially resulting in incorrect radiation doses.
Product
RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B, 2024A including some service packs.
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 (Food)·F-1148-2024·2024-04-17
Deluxe brand Macarons Party Edition recalled for undeclared allergens
Lidl is recalling Deluxe Macarons Party Edition due to undeclared allergens. The packaging is labeled in a foreign language and does not identify wheat, soy, egg, milk, and tree nuts.
Product
Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic container
Category
Food
Distribution
0 states
HighFDA (Food)·F-1127-2024·2024-04-17
Yellow onions recalled due to incomplete botulinum hazard analysis
Pueblo Fruits is recalling 23 cases of yellow onions sold to a single restaurant in Albuquerque because the firm did not complete a hazard analysis for potential Clostridium botulinum growth in vacuum-sealed bags.
Product
Onion Yellow Med 3 Outer Rings 4-5 LB in a 5 LB ,vacuum sealed, clear plastic bag. Labeling: White paper label with the following information attached to the outside of plastic bag. Blake's (Richmond) Onion Yellow Med 3 Outer Rings 4-5 LB PO# 047981 Lot#787806-6883R5, 795046-3948
Category
Food
Distribution
2 states
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
HighFDA (Devices)·Z-1497-2024·2024-04-17
Acetabular Bearing Components Recalled for Marketing Without FDA Clearance
Synovo Production is recalling 1,681 acetabular bearing components that were marketed without FDA clearance.
Product
ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1126-2024·2024-04-17
SWAD Cinnamon Powder Recalled Due to Lead Contamination
RAJA FOODS LLC is recalling SWAD BRAND CINNAMON POWDER (3.5 oz) after testing confirmed lead contamination. The affected batch should not be consumed.
Product
SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case
Category
Food
Distribution
15 states
HighFDA (Food)·F-1131-2024·2024-04-17
Caesar Salad Mislabeled as Garden Salad, Allergens Undeclared
Taylor Farms Southwest recalled 150 units of chicken caesar salad mislabeled as garden salad, with undeclared allergens including egg, fish, and soy. Affected product was distributed in Arizona, Colorado, New Mexico, Nevada, Utah, and Texas.
Product
Family Size Garden Salad 17oz packaged in Flexible plastic combo 32 oz clamshell.
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1516-2024·2024-04-17
PEG feeding tube with blocked connector may impede placement procedure
Boston Scientific's EndoVive 20Fr PEG Kit may have a blocked connector that prevents the guidewire from advancing during placement, potentially causing complications including bleeding and aspiration.
Product
EndoVive 20Fr Push Standard PEG Kit (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: M00568211
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1506-2024·2024-04-17
Chromophare Surgical Light System recalled for insufficient mounting force
Stryker Communications recalls Chromophare Surgical Light Systems due to insufficient mounting force that could compromise the equipment's stability in surgical environments.
Product
Chromophare Surgical Light System , REF CH00000001
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1121-2024·2024-04-17
Nicomex Tequesquite recalled due to elevated lead contamination
Nicomex Inc. is recalling Nicomex Tequesquite seasoning (1.5 oz) due to elevated lead levels. Approximately 192 units were distributed to retailers in New Jersey and New York.
Product
Nicomex Tequesquite, Net Wt. 1.5oz (42.52gms), UPC: 8 8467810180 7. Packaged in a plastic bag.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1488-2024·2024-04-17
Medline SwivAssist Bed Assist Bars Recalled for Safety Standard Non-Compliance
Medline is recalling 79 Bed Assist Bars that failed to comply with federal safety standards for adult portable bed rails. The products were manufactured after the compliance deadline.
Product
Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline SwivAssist Bar, Model Number MDS6800SWIVRH (individual)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0437-2024·2024-04-17
FDA Recalls Rifampin Capsules 300mg Nationwide for Subpotency
Lupin Pharmaceuticals recalls Rifampin Capsules USP 300mg nationwide due to subpotency—the drug contains less active ingredient than labeled. Affected lot: A201064, expiring March 2024. 26,352 bottles involved.
Product
Rifampin Capsules USP, 300mg, 30-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India, NDC 6818-0659-06
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1495-2024·2024-04-17
ConvaTec CarboFlex Wound Dressing Recalled for Failed Sterility Standards
ConvaTec is recalling 63 market units of CarboFlex odor control dressings that fail to meet sterility assurance requirements. Affected lots were distributed in six states.
Product
ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/market unit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1496-2024·2024-04-17
Acetabular Fixation Cups Recalled for Marketing Without FDA Clearance
Synovo Production is recalling 764 acetabular fixation cups marketed without FDA clearance or approval. These hip replacement components were distributed nationwide in Washington state.
Product
ACETABULAR FIXATION CUP, (xx)MM, 5 HOLE, Ti-6AI-4V ELI TiN CERAMIC W/PLASMA SPRAY, STERILEEO, Reference Numbers: 01-01-0554 01-01-0556 01-01-0558 01-01-0560 01-01-0562 01-01-0564 01-01-0566
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2024·2024-04-17
EndoVive 20 Fr Feeding Tube May Obstruct During Placement
Boston Scientific is recalling EndoVive 20 Fr feeding tubes due to potential blockage during placement that may prevent guidewire advancement. This could lead to procedure complications including bleeding, gastric leakage, or aspiration.
Product
EndoVive 20 Fr Safety PEG Push w/ENFit Kit (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: M00509191
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1483-2024·2024-04-17
KWIK-STIK Quality Control Kit Recalled for Fungal Contamination
Microbiologics Inc recalls KWIK-STIK quality control kits contaminated with Aspergillus brasiliensis fungus. Users may observe unexpected fungal growth when using affected control material.
Product
KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for culture media
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2024·2024-04-17
CT Scanner Software Upgrade May Cause Unexpected Table Movement
Philips CT scanner software upgrade may cause the patient tabletop to move unexpectedly during scan initialization, posing collision risk to nearby operators or bystanders.
Product
PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143
Category
Medical Device
Distribution
Distributed nationwide

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13101–13125 of 27722