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

1351–1375 of 39987

HighFDA (Devices)·Z-1697-2026·2026-04-08
da Vinci double fenestrated grasper recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Double Fenestrated Grasper Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including bl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1687-2026·2026-04-08
Artoura ultra high profile expander infusion needles may be blunt
Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc
Category
Medical Device
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 (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-1750-2026·2026-04-08
Paradigm REAL-Time Revel pump delivery varies with pump height changes
Medtronic is recalling Paradigm REAL-Time Revel insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1696-2026·2026-04-08
da Vinci monopolar curved scissors recalled over frayed grip cables
Intuitive Surgical is recalling da Vinci S and Si Monopolar Curved Scissors Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1662-2026·2026-04-08
Philips Allura Xper FD10/10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1711-2026·2026-04-08
Medline anterior hip pack contains recalled Olympus biopsy valves
Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1682-2026·2026-04-08
CPX 4 low height tissue expander infusion needles may be blunt
Mentor is recalling the CPX 4 US Breast Tissue Expander with Suture Tabs, smooth low height 650 cc, 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-157LH Smooth Low Height Tissue Expander, 650cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1737-2026·2026-04-08
Civco eTRAX needle sensor may misreport needle tip position onscreen
Civco is recalling the eTRAX Needle Sensor 16G for Aurora trackers because an inspection and programming error may cause the needle tip position to be incorrectly identified on the user interface.
Product
eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
Category
Medical Device
Distribution
3 states
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-1686-2026·2026-04-08
Artoura breast tissue expander infusion set needles may be blunt
Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2026·2026-04-08
Philips Allura Xper FD20/15 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/15 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15 OR Table; System Code: 722059;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1761-2026·2026-04-08
Burlington Medical leg wraps may lose radiation attenuation over time
Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Leg Wraps.
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-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-1664-2026·2026-04-08
Philips Allura Xper FD20 Biplane X-ray may not start reliably
Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1742-2026·2026-04-08
MiniMed 770G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 770G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2026·2026-04-08
Burlington Medical BAT coverage may lose radiation attenuation over time
Burlington Medical is recalling BAT (Breast, Axilla and Thyroid) Coverage because of the potential for attenuation degradation over time.
Product
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1732-2026·2026-04-08
Civco eTRAX 14G starter kit may misreport needle tip position
Civco is recalling the eTRAX Needle System Starter Kit 14G 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 14G (for Aurora Trackers), Part Number 667-150
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1693-2026·2026-04-08
Sterile radiology procedure kits may have a breached sterile pouch
One lot of Sterile Radiology Procedure Kits, model DYNDH1491B, is being recalled because of a potential breach in the sterile pouch packaging that may compromise sterility.
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2026·2026-04-08
MiniMed 530G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 530G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 530G Insulin Pump (MMT-551, MMT-751)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1765-2026·2026-04-08
Burlington Medical kilt blockers may lose radiation attenuation over time
Burlington Medical is recalling kilt blockers because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Kilt Blockers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1699-2026·2026-04-08
da Vinci grasping retractor instruments recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide

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1351–1375 of 39987