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

26–50 of 589

CriticalFDA (Devices)·Z-1325-2026·2026-02-18
Reprocessed AcuNav catheters recalled over residual material particles inside
Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.
Product
Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH ACUSON AcuNav Ultrasound Catheter, Use on Siemens Systems 10135936RH, 08255790RH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1324-2026·2026-02-18
Reprocessed ultrasound catheters recalled over residual material particles inside
Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1323-2026·2026-02-18
Reprocessed ViewFlex ICE catheters recalled over residual material particles
Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1319-2026·2026-02-18
Reprocessed Webster CS catheters recalled over residual material particles
Medline is recalling 228 units because these lots of reprocessed catheters may contain small particles of residual material.
Product
Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1162-2026·2026-02-11
HOT AXIOS 8mm stents recalled over deployment and expansion problems
Boston Scientific is recalling 150 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 8mm x 8mm, after increased reports of stent deployment and expansion issues.
Product
*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm; Material Number (UPN): M00553530;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1158-2026·2026-02-11
AXIOS stents recalled over deployment and expansion problems during placement
Boston Scientific is recalling 557 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 20mm x 10mm, after increased reports of stent deployment and expansion issues.
Product
AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm; Material Number (UPN): M00553660;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1159-2026·2026-02-11
AXIOS 6mm stents recalled over deployment and expansion problems
Boston Scientific is recalling 39 AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Product
AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1163-2026·2026-02-11
HOT AXIOS 20mm stents recalled over deployment and expansion problems
Boston Scientific is recalling 588 units of the HOT AXIOS Stent and Electrocautery-Enhanced Delivery System, 20mm x 10mm after increased reports of stent deployment and expansion issues.
Product
*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm; Material Number (UPN): M00553560;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1161-2026·2026-02-11
HOT AXIOS stents recalled over deployment and expansion problems
Boston Scientific is recalling 266 HOT AXIOS Stent and Electrocautery-Enhanced Delivery Systems, 6mm x 8mm, after increased reports of stent deployment and expansion issues.
Product
HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm; Material Number (UPN): M00553520;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1160-2026·2026-02-11
AXIOS 8mm stents recalled over deployment and expansion problems
Boston Scientific is recalling 59 units of the AXIOS Stent and Electrocautery-Enhanced Delivery System, 8mm x 8mm after increased reports of stent deployment and expansion issues.
Product
AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm; Material Number (UPN): M00553690;
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1117-2026·2026-02-04
Filled Broselow organizers recalled over potentially harmful dosing errors
SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1114-2026·2026-02-04
Pediatric emergency tapes recalled over potentially harmful drug dosing errors
SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0417-2026·2026-02-04
Pediatric ALS organizers recalled over potentially harmful drug dosing errors
SunMed Holdings is recalling 384 units of the Broselow Domestic Complete ALS Organizer because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
SOMA KITCHEN NATURAL ASAFOETIDA Net Wt. 4 oz (0.25 lb) Product of India Manufactured for and Imported by: Bharat Bazar, Fremont, CA 94539 Use by : JULY-2027 Lot : NATL/ASFTP/G/24 (BB/ASFTP/G/24) UPC : 4 973993 173586 Ingredients :- Natural Hing
Category
Medical Device
Distribution
1 state
CriticalFDA (Devices)·Z-1115-2026·2026-02-04
Broselow Rainbow Tape 7700RE recalled over potentially harmful dosing errors
SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Product
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1014-2026·2026-01-28
Full electric low homecare beds recalled over hand pendants that overheat
Medline is recalling 22,565 units of the Full Electric Low Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
Category
Medical Device
Distribution
4 states
CriticalFDA (Devices)·Z-1016-2026·2026-01-28
Full electric low lightweight homecare beds recalled over overheating pendants
Medline is recalling 15,581 units of the Full Electric Low Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Category
Medical Device
Distribution
4 states
CriticalFDA (Devices)·Z-1147-2026·2026-01-28
Full electric lightweight homecare beds recalled over pendants that may overheat
Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP)…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1012-2026·2026-01-28
Semi electric lightweight homecare beds recalled over pendants that may overheat
Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Category
Medical Device
Distribution
4 states
CriticalFDA (Devices)·Z-1013-2026·2026-01-28
Full electric basic homecare beds recalled over pendants that may overheat
Medline is recalling 138,412 units of the Full Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
Category
Medical Device
Distribution
4 states
CriticalCPSC·26215·2026-01-22
Semi electric homecare beds recalled over hand pendants that may overheat
Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Product
Mikario Trading 5-in-1 Convertible Baby Gyms
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1022-2026·2026-01-21
Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up
Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1021-2026·2026-01-21
Libre 3 Plus sensors recalled in a second lot over carbon build up
Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1023-2026·2026-01-21
Libre 3 Plus sensors recalled over carbon build up causing low readings
Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Product
FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1020-2026·2026-01-21
Glucose monitoring sensors recalled over carbon build up causing low readings
Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Product
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Category
Medical Device
Distribution
36 states
CriticalFDA (Devices)·Z-1000-2026·2026-01-14
Organ recovery packs recalled as not suitable for organ transplant
AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.
Product
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
Category
Medical Device
Distribution
Distributed nationwide

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