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

7576–7600 of 27393

HighFDA (Devices)·Z-2100-2023·2023-07-12
Giraffe OmniBed neonatal devices recalled due to incorrect secondary latch
GE HealthCare is recalling approximately 4,540 Giraffe OmniBed and Giraffe OmniBed Carestation neonatal warming devices worldwide due to potentially incorrect secondary latches on bedside panels.
Product
Giraffe OmniBed Carestation CS1, Model Numbers: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476, g. M1235957, h. M1149051, i. M1146098; Labeled as the following: GIRAFFE OMNIBED CARESTATION CS1, GIRAFFE OMNIBED CARESTATI
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2073-2023·2023-07-12
SurgiMend MP Collagen Matrix Recalled for Endotoxin Testing Issues
TEI Biosciences recalled approximately 3,992 units of SurgiMend MP surgical implants nationwide due to issues with endotoxin testing procedures that may have resulted in unreliable test results.
Product
SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2081-2023·2023-07-12
PriMatrix Ag Fenestrated dermal repair scaffolds recalled for endotoxin testing issues
TEI Biosciences recalled 7,264 units of PriMatrix Ag Fenestrated dermal repair scaffolds nationwide due to possible out-of-specification endotoxin test results caused by testing methodology defects.
Product
PriMatrix Ag Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2089-2023·2023-07-12
DeRoyal Pelvic Exam Trays Recalled Due to Compromised Package Seals
DeRoyal Industries is recalling 3 packs of Pelvic Exam Trays because the outer package seals may be open or compromised, potentially affecting the sterility of the medical procedure packs.
Product
Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY, REF 89-6219
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2074-2023·2023-07-12
SurgiMend 3.0 Soft Tissue Graft Recalled for Endotoxin Testing Defect
SurgiMend 3.0 collagen matrix is being recalled nationwide (13,390 units) due to possible endotoxin contamination from deficiencies in endotoxin testing procedures.
Product
SurgiMend 3.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x20 cm, 20x25 cm, 1x5 cm, 10x25 cm 4x7cm Fenestrated, and 10x25 cm Fenestrated.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2064-2023·2023-07-12
Surgical drill guides may bend and produce metal shavings during use
T.A.G. MEDICAL PRODUCTS CORPORATION is recalling Betta Link LG Reusable ProngED Guides used in orthopedic surgery because the guides may bend when force is applied, creating metal shavings that could injure patients.
Product
Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2061-2023·2023-07-12
BETTA LINK LG Implant Drill Guide Bending Risk
T.A.G. MEDICAL PRODUCTS is recalling BETTA LINK LG KNOTLESS IMPLANT KIT because drill guides may bend during surgical use, potentially creating metal shavings that could injure patients.
Product
BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045160
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1927-2023·2023-07-05
Endotracheal Tubes Recalled for Connector Disconnection Risk
Teleflex LLC is recalling 2,860 endotracheal tubes due to reports of 15mm connector disconnection. Affected tubes were distributed nationwide including Puerto Rico.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1994-2023·2023-07-05
MEGADYNE MEGA 2000 Patient Return Electrode Recalled Due to Patient Burns
The FDA is recalling 21,100 units of the MEGADYNE MEGA 2000 Patient Return Electrode due to reports of patient burns during electrosurgical procedures. All units distributed nationwide are affected.
Product
MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1841-2023·2023-07-05
Slick Set Uncuffed Endotracheal Tube Connector Disconnection Recall
Teleflex LLC is recalling approximately 10,650 units of Slick Set Uncuffed Endotracheal Tubes due to reports of 15mm connector disconnection from the tube.
Product
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2000-2023·2023-07-05
MEGADYNE MEGA SOFT Return Electrode Recalled for Burns During Surgical Procedures
Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode due to reported patient burns that occurred during electrosurgical procedures.
Product
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1893-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk
Teleflex is recalling 18,620 endotracheal tubes due to reported disconnection of 15mm connectors. The tubes are used for oral and nasal intubation and were distributed nationwide.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1999-2023·2023-07-05
MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode Recalled for Patient Burns
Megadyne Medical Products is recalling 21,100 units of MEGA SOFT Universal Plus Patient Return Electrodes used in electrosurgery. The FDA Class I recall follows reports of patient burns during surgical procedures.
Product
MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1898-2023·2023-07-05
RUSCHELIT Safety Clear Tracheal Tube 15mm Connector Disconnection Recall
TELEFLEX is recalling RUSCHELIT Safety Clear Tracheal Tubes due to reported disconnection of the 15mm connector, affecting approximately 37,076 units distributed nationwide.
Product
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1874-2023·2023-07-05
Endotracheal Tube Recall Due to 15mm Connector Disconnection
TELEFLEX is recalling endotracheal tubes due to reports of 15mm connector disconnection. Approximately 25,160 units were distributed nationwide.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1890-2023·2023-07-05
Teleflex endotracheal tubes recalled for connector disconnection defect
Teleflex LLC is recalling 170,179 endotracheal tubes nationwide due to reports of 15mm connector disconnection. The tubes are used for airway management in medical facilities.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082080
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1947-2023·2023-07-05
Preformed AGT Endotracheal Tubes Recalled Due to Connector Disconnection
Teleflex is recalling 25,520 Preformed AGT endotracheal tubes due to reports of 15mm connector disconnection. This is an FDA Class I recall affecting units distributed nationwide.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1828-2023·2023-07-05
Teleflex Slick Set endotracheal tubes recalled for connector disconnection
Teleflex Slick Set endotracheal tubes (REF 170055) are being recalled by the FDA following reports of disconnection of the 15mm connector. This Class I recall affects approximately 3,530 units distributed nationwide.
Product
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1876-2023·2023-07-05
Endotracheal Tube Connector Disconnection Recall — FDA Class I
TELEFLEX endotracheal tubes (Murphy design) may have a disconnected 15mm connector. Approximately 12,382 affected units were distributed nationwide. Healthcare facilities should inspect tubes before use.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1882-2023·2023-07-05
TELEFLEX Endotracheal Tubes Recalled Due to Connector Disconnection Risk
TELEFLEX is recalling 760 endotracheal tubes due to reports of 15mm connector disconnection. This medical device failure could compromise airway management during critical care.
Product
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1953-2023·2023-07-05
Endotracheal Tubes Recalled for Potential 15mm Connector Disconnection
TELEFLEX LLC is recalling Preformed AGT Oral Endotracheal Tubes because the 15mm connector may disconnect from the tube, creating a potential airway access risk.
Product
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1938-2023·2023-07-05
TELEFLEX Endotracheal Tubes Recalled for 15mm Connector Disconnection
TELEFLEX is recalling 5,600 endotracheal tubes nationwide due to reports of 15mm connector disconnection that could compromise airway management during patient care.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1888-2023·2023-07-05
Endotracheal Tubes Recalled Due to Connector Disconnection Risk
TELEFLEX endotracheal tubes are being recalled due to reports of the 15mm connector disconnecting from the tube. The recall affects 860,472 units distributed nationwide, including Puerto Rico.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1833-2023·2023-07-05
Teleflex Slick Set Endotracheal Tube Connector Disconnection Recall
Teleflex is recalling Slick Set Cuffed Endotracheal Tube and Stylet Sets due to reports of disconnection of the 15mm connector from the endotracheal tube. The affected units were distributed nationwide.
Product
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1899-2023·2023-07-05
RUSCHELIT Safety Clear Tracheal Tubes Recalled for Connector Disconnection
TELEFLEX LLC recalls RUSCHELIT Safety Clear Tracheal Tubes due to reports of 15mm connector disconnection. The Class I recall affects 30,391 units distributed nationwide including Puerto Rico.
Product
RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480045
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

7576–7600 of 27393