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

5201–5225 of 27204

HighFDA (Devices)·Z-2451-2025·2025-09-03
[pending] Akreos, SKU: AO60P0300. Akreos intraocular lenses
Pending LLM rewrite. Source: FDA_DEVICE Z-2451-2025.
Product
Akreos, SKU: AO60P0300. Akreos intraocular lenses
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2476-2025·2025-09-03
[pending] STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Fibrinogen 5 kit is intended for use
Pending LLM rewrite. Source: FDA_DEVICE Z-2476-2025.
Product
STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Fibrinogen 5 kit is intended for use with the analyzers of the STA-R, STA Compact and STA Satellite families for the quantitative determination of fibrinogen levels in human citrated plasma by the clotting method of
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2453-2025·2025-09-03
[pending] BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD P
Pending LLM rewrite. Source: FDA_DEVICE Z-2453-2025.
Product
BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD PhaSeal Injector Lu63er Lock (N35C Multi), REF: 515005 BD PhaSeal Protector (P14), REF: 515100 BD PhaSeal Protector (P21), REF:
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2362-2025·2025-09-03
[pending] C9-3v Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2362-2025.
Product
C9-3v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2443-2025·2025-09-03
[pending] Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, s
Pending LLM rewrite. Source: FDA_DEVICE Z-2443-2025.
Product
Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2472-2025·2025-09-03
[pending] AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MOD
Pending LLM rewrite. Source: FDA_DEVICE Z-2472-2025.
Product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ANTERIOR HIP PACK, MODEL/ITEM NUMBER AMAH40N; 2)TOTAL KNEE DAN MYER, MODEL/ITEM NUMBER CCKM67F; 3)HIP PROTHESIS PACK, MODEL/ITEM NUMBER HSTH03N; 4)DTC ANTERIOR HIP PACK (PS 209459), MODEL/ITEM NUM
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2399-2025·2025-09-03
[pending] S9-2 Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2399-2025.
Product
S9-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0598-2025·2025-09-03
[pending] SUCRALFATE (SUCRALFATE)
Pending LLM rewrite. Source: FDA_DRUG D-0598-2025.
Product
SUCRALFATE — SUCRALFATE (SUCRALFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2424-2025·2025-09-03
[pending] ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3
Pending LLM rewrite. Source: FDA_DEVICE Z-2424-2025.
Product
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2442-2025·2025-09-03
[pending] Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad, a screw, lens cleaning wipe,
Pending LLM rewrite. Source: FDA_DEVICE Z-2442-2025.
Product
Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2475-2025·2025-09-03
[pending] STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended
Pending LLM rewrite. Source: FDA_DEVICE Z-2475-2025.
Product
STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2404-2025·2025-09-03
[pending] V9-2 Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2404-2025.
Product
V9-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2416-2025·2025-09-03
[pending] Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Produc
Pending LLM rewrite. Source: FDA_DEVICE Z-2416-2025.
Product
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature fo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2395-2025·2025-09-03
[pending] S7-3t Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2395-2025.
Product
S7-3t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2374-2025·2025-09-03
[pending] L12-4 Lumify Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2374-2025.
Product
L12-4 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0527-2025·2025-09-03
[pending] Paneer Cheese, Net Wt. 30 lbs., packaged in 5 lb. vacuum-sealed plastic bags with lot code 2517061,
Pending LLM rewrite. Source: FDA_FOOD H-0527-2025.
Product
Paneer Cheese, Net Wt. 30 lbs., packaged in 5 lb. vacuum-sealed plastic bags with lot code 2517061, packed 6 bags per white cardboard case with packed on date 6-18-25, distributed for food service only
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2406-2025·2025-09-03
[pending] X11-4t Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2406-2025.
Product
X11-4t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2471-2025·2025-09-03
[pending] AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL
Pending LLM rewrite. Source: FDA_DEVICE Z-2471-2025.
Product
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2391-2025·2025-09-03
[pending] S4-1 Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2391-2025.
Product
S4-1 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2392-2025·2025-09-03
[pending] S4-1 Lumify Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2392-2025.
Product
S4-1 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2378-2025·2025-09-03
[pending] L15-7IO TRANSDUCER Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2378-2025.
Product
L15-7IO TRANSDUCER Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2356-2025·2025-09-03
[pending] C6-3 Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2356-2025.
Product
C6-3 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2409-2025·2025-09-03
[pending] X5-1c Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2409-2025.
Product
X5-1c Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2400-2025·2025-09-03
[pending] SCNHD LA L7-4 HDI Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2400-2025.
Product
SCNHD LA L7-4 HDI Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2363-2025·2025-09-03
[pending] C9-4 Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2363-2025.
Product
C9-4 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide

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5201–5225 of 27204