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

2426–2450 of 89459

HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0410-2026·2026-04-08
Quality Choice moisturizing relief eye drops recalled over sterility assurance
Quality Choice Moisturizing Relief Eye Drops, containing dextran 70, polyethylene glycol 400, povidone and tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS — QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1734-2026·2026-04-08
Civco eTRAX 18G starter kit may misreport needle tip position
Civco is recalling the eTRAX Needle System Starter Kit 18G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified.
Product
eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1766-2026·2026-04-08
Oxoid Microbact Listeria kit may identify the incorrect organism
Oxoid, part of Thermo Fisher Scientific, is recalling one lot of the Microbact 12L Listeria identification kit because it may identify the incorrect organism.
Product
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1695-2026·2026-04-08
Olympus SOLTIVE Pro laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Pro SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0413-2026·2026-04-08
GoodSense original formula eye drops recalled over sterility assurance
GoodSense Eye Drops Original Formula, containing tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
GOODSENSE EYE DROPS ORIGINAL FORMULA — GOODSENSE EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1710-2026·2026-04-08
Medline bronchoscopy kits contain Olympus biopsy valves that shed fragments
Medline is recalling six bronchoscopy and thoracic kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I 5. KIT, WR THORACIC, DYNJ911252 6. LARYNGOSCOPY/BRON
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0411-2026·2026-04-08
Artificial tears glycerin drops recalled over lack of sterility assurance
Artificial Tears containing glycerin are being recalled for lack of assurance of sterility. About 1,023,096 bottles were distributed nationwide.
Product
ARTIFICIAL TEARS — ARTIFICIAL TEARS (GLYCERIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2026·2026-04-08
Burlington Medical kilts may lose radiation attenuation over time
Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Kilt
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2026·2026-04-08
MiniMed 780G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 780G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1674-2026·2026-04-08
Philips Azurion 3 M15 X-ray may not start from foot switch
Philips is recalling the Azurion 3 M15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2026·2026-04-08
CPX 4 medium height tissue expander infusion needles may be blunt
Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth medium height range because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2026·2026-04-08
Philips Allura Xper FD10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1679-2026·2026-04-08
Philips Azurion 5 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M12; System Code: (1)722227, (2)722231;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1659-2026·2026-04-08
Philips Allura Xper FD10C X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD10C; System Code: 722001;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1676-2026·2026-04-08
Philips Azurion 7 B20 X-ray may not start from foot switch
Philips is recalling the Azurion 7 B20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1667-2026·2026-04-08
Philips Allura Xper FD10 OR Table X-ray may not start reliably
Philips is recalling the Allura Xper FD10 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1677-2026·2026-04-08
Philips Azurion 7 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 7 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1673-2026·2026-04-08
Philips Azurion 3 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 3 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2026·2026-04-08
Philips Azurion 7 B12 X-ray may not start from foot switch
Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1666-2026·2026-04-08
Philips Allura Xper FD20 Biplane OR Table X-ray may not start
Philips is recalling the Allura Xper FD20 Biplane OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1668-2026·2026-04-08
Philips Allura Xper FD20/10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/10; System Code: 722029;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1669-2026·2026-04-08
Philips Allura Xper FD20/20 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20; System Code: 722038;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1660-2026·2026-04-08
Philips Allura Xper FD10F X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10F because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10F; System Code: 722002;
Category
Medical Device
Distribution
Distributed nationwide

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2426–2450 of 89459