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

8876–8900 of 13683

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-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-2101-2023·2023-07-12
Giraffe OmniBed neonatal incubator recall due to incorrect secondary latch installation
GE HealthCare is recalling Giraffe OmniBed neonatal incubators with potentially incorrect secondary latches on bedside panels. An incorrect latch type may have been installed on northeast and/or northwest panels of affected units.
Product
Giraffe OmniBed, with the following Model Numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, 6650-0094-901, 6650-0001-9901, 6650-0029-901, 6650-0080-901, 6650-0032-901, 6650-0077-901, 6650-001-901, 6650-0006-901, 6650-0129-901, 6650-0063-902, 6650-0130-901, 6650
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2057-2023·2023-07-12
TrackMaster GE Treadmill Recall Due to Drive Circuit Board Malfunction
Full Vision Inc is recalling 1,416 TrackMaster GE T2100-ST2 220V treadmills worldwide due to a drive circuit board defect that can cause the treadmill to stop suddenly, reverse unexpectedly, or accelerate forward, posing a risk of falls or injury.
Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2023·2023-07-12
Collagen surgical matrix recalled for potential endotoxin testing issues
TEI Biosciences is recalling 9,215 units of SurgiMend PRS Meshed, a surgical collagen matrix, due to possible out-of-specification endotoxin test results.
Product
SurgiMend PRS Meshed; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Size 10cm x 20cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2085-2023·2023-07-12
Soft tissue repair matrix recalled due to possible endotoxin contamination
TEI Biosciences is recalling 4,832 units of TissueMend Advanced Soft Tissue Repair Matrix due to possible out-of-specification endotoxin test results. No illnesses or injuries have been reported.
Product
TissueMend; Advanced Soft Tissue Repair Matrix; Rx Only; Sizes 5x6 cm, 6x10 cm, and 3x3 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2059-2023·2023-07-12
Fenestrated Graspers Recalled Due to Potential Breakage and Fragment Risk
Intuitive Surgical is recalling 46,033 da Vinci Xi/X Tip-Up Fenestrated Graspers worldwide due to a manufacturing issue that can cause grip breakage, potentially allowing stainless steel fragments to enter the patient.
Product
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2093-2023·2023-07-12
COVID-19 Test Strips Recalled for Lot Number Label Discrepancy
NeuMoDx SARS-CoV-2 test strips from lot 123909 have conflicting lot numbers between the package label and barcode label that the instrument reads.
Product
NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP). RE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2084-2023·2023-07-12
Collagen matrix recalled for endotoxin testing methodology issues
TEI Biosciences recalled 665 units of Revize-X collagen matrix nationwide due to possible out-of-specification endotoxin test results caused by issues with the company's testing procedures. No illnesses have been reported.
Product
Revize-X; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 12x6 cm and 10x9 cm.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2071-2023·2023-07-12
SurgiMend collagen matrices recalled for endotoxin test result quality issues
TEI Biosciences recalls SurgiMend 1.0 collagen matrices due to problems with endotoxin testing procedures that may have produced inaccurate test results. 52 units were distributed nationwide.
Product
SurgiMend 1.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 18x12 cm Thin and 10x15 cm Thin.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2095-2023·2023-07-12
Teleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions
TELEFLEX LLC recalled the Pilling O'REILLY ESOPHAGEAL RETRACTOR (REF 381801A) due to incomplete pre-cleaning instructions in the product's Instructions for Use. The recall affects 365 units distributed nationwide and internationally.
Product
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2092-2023·2023-07-12
NexGen Tibial Plate Recalled for Incorrect Outer Packaging Label
Zimmer, Inc. is recalling NexGen Precoat Stemmed Tibial Plate Size 5 devices due to incorrect outer packaging labeling. Affected units were distributed internationally in India.
Product
NexGen Precoat Stemmed Tibial Plate Size 5
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2096-2023·2023-07-12
Teleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions
Teleflex LLC is recalling 170 units of the Pilling Lowsley Prostatic Retractor due to incomplete pre-cleaning instructions in the user manual. Incomplete instructions may prevent proper sterilization of the surgical instrument.
Product
Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2098-2023·2023-07-12
KLS Martin Battery Packs Recalled for Switched Expiration Date Labels
Pro-Dex Inc recalls KLS Martin Battery Packs used in surgical screwdrivers due to manufacturing and expiration dates being reversed on sterile pouch labels, causing batteries to appear prematurely expired.
Product
KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
Category
Medical Device
Distribution
1 state
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-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
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-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-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-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-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-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-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-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-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

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8876–8900 of 13683