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

351–375 of 5100

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 (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-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), non-inv
Category
Medical Device
Distribution
Distributed nationwide
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
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-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
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-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-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-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-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-1001-2026·2026-01-14
Organ recovery surgical packs recalled as not suitable for organ transplant
AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Product
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1002-2026·2026-01-14
Mini Plus surgical kits recalled as not suitable for organ transplant
AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.
Product
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Category
Medical Device
Distribution
Distributed nationwide
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
CriticalFDA (Devices)·Z-0933-2026·2025-12-31
Vapor 2000 anesthetic vaporizers recalled over an out of specification component
Draeger is recalling 431 Vapor 2000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.
Product
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0934-2026·2025-12-31
Vapor 3000 anesthetic vaporizers recalled over an out of specification component
Draeger is recalling 188 Vapor 3000 anesthetic vaporizers because a certain component was not delivered within specification and contained impurities. The action is Class I.
Product
Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0939-2026·2025-12-31
Ophthalmic surgical packs recalled over incomplete seals affecting sterility
Alcon Research is recalling 151 Custom Pak ophthalmic procedure packs because the packs may have incomplete seals affecting sterility. The FDA has classified the action as Class I.
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Numbers: 9903-20, 17188-04, 19762-03, 19203-04, 19203-04, 17957-10 Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience k
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0914-2026·2025-12-24
Carestation 750 anesthesia systems recalled over potential unexpected shutdown
GE Medical Systems is recalling 888 Carestation 750 series anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The action is Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 750 A1, REF 1012-9750-000; Carestation 750 A2, REF 1012-9750-002; Carestation 750c A1, REF 1012-9755-000; Products for which affected PMB can be used as a spare part: Carestatio
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0885-2026·2025-12-24
Infusion pump software recalled over anomalies that could cause serious harm
Fresenius Kabi USA is recalling Ivenix Infusion System LVP software versions 5.10.1 and earlier, which the firm states contain anomalies with the potential to cause serious patient harm or death.
Product
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.
Category
Medical Device
Distribution
20 states
CriticalFDA (Devices)·Z-0915-2026·2025-12-24
Anesthesia power management boards recalled over potential unexpected system shutdown
GE Medical Systems is recalling 203 Carestation anesthesia system Power Management Board field replaceable units over potential unexpected shutdown if AC mains power is lost.
Product
GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0913-2026·2025-12-24
Anesthesia systems recalled over potential unexpected shutdown on mains power loss
GE Medical Systems is recalling 1,277 Carestation anesthesia systems over potential unexpected shutdown if AC mains power is unplugged or fails. The FDA has classified the action as Class I.
Product
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF 1012-9620
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0591-2026·2025-12-17
Ventilator airway connectors recalled after cracks formed in the hose
Draeger is recalling 191,470 ErgoStar CM 45 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states
CriticalFDA (Devices)·Z-0592-2026·2025-12-17
ErgoStar CM 55 airway connectors recalled after cracks formed in the hose
Draeger is recalling 118,850 ErgoStar CM 55 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states
CriticalFDA (Devices)·Z-0593-2026·2025-12-17
ErgoStar CM 60 airway connectors recalled after cracks formed in the hose
Draeger is recalling 2,050 ErgoStar CM 60 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
Category
Medical Device
Distribution
10 states
CriticalFDA (Food)·H-0252-2026·2025-12-17
ErgoStar CM 40 airway connectors recalled after cracks formed in the hose
Draeger is recalling 14,420 ErgoStar CM 40 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Product
Deep-brand Premium Select Chikoo Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
Category
Medical Device
Distribution
0 states

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351–375 of 5100