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

7301–7325 of 89525

HighFDA (Food)·F-0732-2025·2025-04-30
MO-CHA Premium Non-Dairy Creamer Recalled for Undeclared Milk Allergen
MO-CHA brand Premium Non-Dairy Creamer is recalled because the label does not declare milk as an allergen, despite milk being present in the product. Consumers with milk allergies are at risk of adverse reaction.
Product
MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein, Emulsifier (471, 481i), Stabilizer(340ii, 452i), Anti-caking agent(551), Food flavor; Shelf Life: 24 months; Net Weight (NET WT): 2.2 lbs (1kg); IMPORTED BY Momo
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1654-2025·2025-04-30
Abbott CELL-DYN Ruby hematology analyzer affected by expired reagent date masking
Abbott is recalling the CELL-DYN Ruby hematology analyzer because expired reagents may have their expiration dates automatically changed to current or future dates without user notification, potentially leading to use of expired reagents.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-10 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1650-2025·2025-04-30
InPen Smart Insulin Pen Recall Due to Incorrect Assembly
Medtronic MiniMed is recalling InPen smart insulin pens that may have been incorrectly assembled, potentially causing the insulin cartridge to not fit or the cartridge holder to be difficult to remove. Users without backup insulin could experience temporary hyperglycemia.
Product
InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
Category
Medical Device
Distribution
41 states
HighFDA (Food)·F-0729-2025·2025-04-30
Spermidine Dietary Supplement Recalled for Undeclared Wheat Allergen
Supplement Manufacturing Partner Inc. is recalling Spermidine Maximum Strength 10 mg dietary supplement (Lot 12792402-44) because it contains undeclared wheat, a major allergen not listed on the label.
Product
Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellu
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-1655-2025·2025-04-30
CELL-DYN Ruby hematology analyzer system expiration date validation
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers (model 08H67-13) because expired reagents can be used without proper notification when their expiration dates are scanned or entered into the system.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-13 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1656-2025·2025-04-30
CELL-DYN Ruby hematology analyzer medical device recall
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because expired reagents may be used without user notification when scanned or manually entered into the system, contrary to manufacturer guidelines.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 04U42-84 Software Version: All software versions Product Description: CELL-DYN Ruby
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1623-2025·2025-04-30
Medtronic NIM Vital Nerve Monitoring System Software Version Recall
Medtronic is recalling NIM Vital Nerve Monitoring Systems with software versions v1.6.4 or earlier due to potential increased stimulus artifact that may require troubleshooting and could lead to procedure delay, extubation, and medical intervention.
Product
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED, REF: NIM4CM01RF; PATIENT INTERFACE NIM4CPB1 NIM 4.0, REF: NIM4CPB1; PATIENT INTFC NIM4CPB1RF NIM 4.0 REFURB, REF: NIM4CPB1RF; SOFTWARE NIM4SWU143 UPGRA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1639-2025·2025-04-30
BD PYXIS MEDBANK Automated Dispensing Cabinet Software Defect
CareFusion's BD PYXIS MEDBANK and MEDFLEX automated dispensing cabinets may experience a software issue during bin restocking that doubles bin quantities, potentially delaying access to medications and supplies.
Product
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-1HM-1FM, 169-102; MINI 2FH, 138902-01; MINI 2FH, 169-104; MINI 2FM, 169-105; MINI 2HH-1FH, 169-106; MINI 2HH-1FH, 138908-01; MINI 2HH-1FM, 169-107; MINI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1652-2025·2025-04-30
CELL-DYN Ruby Hematology Analyzer Expiration Date Software Defect
Abbott's CELL-DYN Ruby hematology analyzer may accept expired reagents without alerting the operator, potentially allowing use of expired materials in patient testing.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1653-2025·2025-04-30
CELL-DYN Ruby hematology analyzer expiration date software defect
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because a software defect allows expired reagents to be used without user notification. The system may incorrectly update expiration dates to current or future dates, contrary to the operator's manual.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-03 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1651-2025·2025-04-30
Stryker Latitude EV Humeral Revision Stem Trial with Incorrect Marking
A specific lot of Stryker Latitude Humeral Trial Stems has incorrect laser marking and color indicator, potentially resulting in implantation of the wrong device size and orientation.
Product
stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1669-2025·2025-04-30
Rover Mobile X-ray System internal fastening mechanism failure potential
Micro-X Ltd. is recalling Rover Mobile X-ray System units (models MXU-RV71, MXU-RV35) due to a potential failure of the internal fastening mechanism within the generator. Affected units were distributed in New Jersey, Washington, and Puerto Rico.
Product
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring med
Category
Medical Device
Distribution
3 states
HighFDA (Food)·F-0720-2025·2025-04-30
Chicken Salad Recalled Due to Undeclared Milk Allergen
Cromer Food Services is recalling chicken salad sandwiches because milk was not declared on the label. Consumers with milk allergies are at risk.
Product
CFS CROMER FOOD SERVICES, INC. Anderson, SC 29621 CHICKEN SALAD On White NET WT. 4.3 OZ CONTAINS: EGGS, WHEAT, SOY UPC 31166 & UPC 13172
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1582-2025·2025-04-30
Veradius Unity wireless foot switch pedal may emit unintended radiation
Philips North America is recalling Veradius Unity foot switch pedals that may become stuck in the active position, causing unintended radiation emission during medical procedures.
Product
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0734-2025·2025-04-30
S Martinelli Apple Juice Recalled for Potential Patulin Contamination
S Martinelli & Company is recalling approximately 7,234 cases of apple juice in 10 oz bottles due to potential contamination with patulin. Consumers who have purchased affected product should not consume it.
Product
Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)
Category
Food
Distribution
28 states
HighFDA (Devices)·Z-1657-2025·2025-04-30
Globus Medical MAGEC 2 Rod recalled for incorrect outer diameter assembly
Globus Medical is recalling MAGEC 2 Rod model MC2-5090S devices because certain units were assembled with a 5.5mm outer diameter rod instead of the required 5.0mm specification.
Product
MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1583-2025·2025-04-30
Zenition 70 Medical Device Recall: Unintended Radiation Exposure Risk
Philips is recalling Zenition 70 systems with Vascular Extension option and Wireless Foot Switch due to potential for unintended radiation exposure in healthcare facilities.
Product
Zenition 70. The device is to be used in health care facilities both inside and outside the operating room, sterile as well as non-sterile environment in a variety of procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0733-2025·2025-04-30
Magic Flame Hulled Sunflower Kernels Bakery Grade Recall
JJ Nuts, LLC is recalling Magic Flame Hulled Sunflower Kernels due to glass fragments found in the finished product.
Product
MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. Bag, Three ply Paper bags, 1100 Paper bags x 50 Ib. on 20 pallets. Store in dry warehouse, room temperature
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1580-2025·2025-04-30
Zenition 50 Medical Imaging Devices Wireless Foot Switch Recall
Philips is recalling Zenition 50 medical imaging devices because the wireless foot switch pedal may get stuck in the active position, causing unintended radiation emission.
Product
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1663-2025·2025-04-30
Skytron Freedom Monitor Mount Hardware Recall for Inadequate Thread Engagement
The mounting hardware supplied with the Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount does not provide adequate thread engagement to support the weight of the frame and monitor, creating a risk of hardware failure and separation.
Product
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1670-2025·2025-04-30
Rover Mobile X-ray System internal fastening mechanism failure risk
Micro-X Ltd. is recalling the Rover Mobile X-ray System (model MXU-RV35) due to a potential failure of the internal fastening mechanism within the generator. Five units distributed in New Jersey, Washington, and Puerto Rico are affected.
Product
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagno
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1660-2025·2025-04-30
Philips Brilliance CT Big Bore X-Ray System Gantry Motion Collision Hazard
Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.
Product
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1622-2025·2025-04-30
VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System C-Ring Break
Maquet Cardiovascular is recalling the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to a ceramic C-Ring component that may break during use. At least 12 user complaints were reported as of March 3, 2025.
Product
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The Harvesting Cannula has four lumens which house the endoscope, C-Ring, distal lens washer tube, and Harvesting Tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0737-2025·2025-04-30
Cuban-Style Black Bean Soup recalled for potential wood contamination
Request Foods Incorporated is recalling Cuban-Style Black Bean Soup due to potential contamination with wood. The product was distributed in Illinois and Michigan.
Product
Cuban-Style Black Bean Soup, 4 / 4lb pouches, Net Wt. 16lb
Category
Food
Distribution
2 states
SevereNHTSA·25V279000·2025-04-29
Temsa Recalls TS30, TS35, and TS45 Buses Due to Brake Overheating Risk
Temsa is recalling 2021-2026 TS30, TS35, and TS45 buses because a temporary bus stop valve may activate unintentionally, causing brakes to overheat and increasing fire risk.
Product
TEMSA — TEMSA TS30, TS35, TS45
Category
Vehicle
Distribution
Distributed nationwide

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7301–7325 of 89525