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 the agency’s own highest classification or reported deaths or serious injuries, 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

776–800 of 27681

HighFDA (Devices)·Z-2342-2026·2026-06-17
MIC Safety 20 Fr push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2408-2026·2026-06-17
Halyard towel six packs shipped without validated sterilization in Iowa
Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.
Product
Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2212-2026·2026-06-10
Pediatric care bed KayserBett IDA recalled due to entrapment hazard
KayserBett IDA pediatric care beds are being recalled because the hand control can be operated by children, creating a risk of entrapment and serious injury or death.
Product
Pediatric care bed; Product Designation: KayserBett IDA;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2224-2026·2026-06-10
Ivenix infusion pumps may hide internal damage after being dropped
Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.
Product
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Category
Medical Device
Distribution
21 states
SevereFDA (Devices)·Z-2277-2026·2026-06-10
Spinocan spinal needle kits recalled over Huons bupivacaine quality issues
Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.
Product
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211)…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2250-2026·2026-06-10
BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2026·2026-06-10
BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2255-2026·2026-06-10
BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine
BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2208-2026·2026-06-10
Atlan A350XL anesthesia workstations may fail during mechanical ventilation
Atlan A350XL anesthesia workstations are being recalled because units either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Product
Atlan A350XL. Model Number: 8621600. anesthesia workstation
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-2278-2026·2026-06-10
Design Options spinal trays recalled over Huons bupivacaine quality issues
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
Product
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2254-2026·2026-06-10
BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2248-2026·2026-06-10
BD Quincke spinal trays recalled over Huons bupivacaine quality issues
BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2276-2026·2026-06-10
B. Braun spinal needle kits recalled over Huons bupivacaine quality issues
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Product
Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868)…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2256-2026·2026-06-10
BD spinal trays recalled as a sub-recall of Huons bupivacaine
BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2207-2026·2026-06-10
Atlan A350 anesthesia workstations may fail during mechanical ventilation
Atlan A350 anesthesia workstations are being recalled because units either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Product
Atlan A350. Model Number: 8211500. anesthesia workstation
Category
Medical Device
Distribution
11 states
SevereFDA (Devices)·Z-2252-2026·2026-06-10
BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2253-2026·2026-06-10
BD combined Whitacre and Quincke spinal trays recalled over bupivacaine
BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2257-2026·2026-06-10
BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2251-2026·2026-06-10
BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2223-2026·2026-06-10
Ivenix pump software may report false battery health and shut down
The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.
Product
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2291-2026·2026-06-10
Philips Azurion 7M20 Roadmap Pro may produce unusable dark images
Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2026·2026-06-10
Avanta administration tube sets may not engage the flow control valve
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
Product
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2026·2026-06-10
Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Product
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2262-2026·2026-06-10
Baxter Exacta Mix inlet sets may contain incorrect 0.8-micron filters
Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.
Product
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2026·2026-06-10
BD Pyxis MedBank Mini fingerprint scanner may overheat and burn
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide

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