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

16026–16050 of 27500

HighFDA (Devices)·Z-1315-2019·2019-05-22
R82 Wombat Living Activity Chair Recalled for Plastic Joint Breakage
R82 A/S is recalling 68 Wombat Living activity chairs (wheelchairs) in North Carolina due to reports of the plastic joint connecting the back to the seat breaking.
Product
Wombat Living, Size 3, Item Numbers: 953121-00, 953126-00, 953131-00, 953132-00, 935-135-00, 935136-00, 953211-00, 953221-00, 953222-00, 953225-00, 953226-00, 953231-001, 953232-00, 953236-00 Product Usage: Activity chair (wheelchair)
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1323-2019·2019-05-22
Philips SureSigns VS4 Monitor Software Defect Recall
Philips is recalling SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS4 NBP, SpO2, Product Number 863283. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1331-2019·2019-05-22
Shippert Medical Technologies Recalls Tissu-Trans FILTRON 250 Due to Pouch Integrity Concerns
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 250 sterile filters because the pouch integrity cannot be assured without visual examination.
Product
Tissu-Trans FILTRON 250, Catalog 3-TT-FILTRON 250, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2019·2019-05-22
Ethicon Endo-Surgery Recalls 33 mm Endoscopic Curved Intraluminal Staplers
Ethicon Endo-Surgery Inc is recalling 434,614 Model ECS33A staplers worldwide because they may have an insufficient firing stroke to break the washer and form staples.
Product
Endoscopic Curved Intraluminal Stapler, 33 mm diameter, Model ECS33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1327-2019·2019-05-22
Pentax Medical C2 CryoBalloon Catheter Recalled for Dose Transmission Error
PENTAX of America Inc is recalling 4 C2 CryoBalloon Catheters because incorrect default doses and increments may be transmitted to the controller if the RFID tag is not correctly readable.
Product
Pentax Medical C2 CryoBalloon Standard 90 degree Catheter, Model FG 1030, Sterile, RX. Product Usage: The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of…
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-1317-2019·2019-05-22
Philips SureSigns VS3 NBP Recall for Pulse Rate Measurement Limitation
Philips is recalling SureSigns VS3 NBP monitors because software prevents the display and alarm for pulse rates above 240 beats per minute.
Product
SureSigns VS3 NBP, Product Number 863069. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1342-2019·2019-05-22
Siemens Artis Q Angiography Systems Recalled for Tabletop Movement Blockage
Siemens is recalling 459 Artis Q angiography systems because the floating tabletop may become blocked after a collision sensor activates.
Product
Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1296-2019·2019-05-15
Abbott ARCHITECT cSystems ICT Module Recall for False Chloride Results
Abbott is recalling ARCHITECT cSystems ICT Modules due to a potential for falsely elevated serum or plasma chloride results.
Product
Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip Technology) is used for the quantitation of sodium, potassium, and chloride in human serum, plasma, or urine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling specific lots of the Anchor Tissue Retrieval System because seal defects may compromise the product's sterility.
Product
ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TRS-ROBO-8 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2019·2019-05-15
Siemens Cios Alpha C-arm X-ray System Recalled for Component Wear
Siemens is recalling two Cios Alpha mobile X-ray systems because continuous high-output operation may cause premature failure of radiation components.
Product
Cios Alpha with software version VA30-mobile C-arm x-ray Material # 11105200 Product Usage: The Cios Alpha is a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1302-2019·2019-05-15
Zimmer Biomet Recalls T7 Driver Cannulated AO Due to Fracture Risk
Zimmer Biomet is recalling 5,885 T7 Driver Cannulated AO units because they may fracture, bend, or shear during use.
Product
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall affects 7,930 units distributed in the US and 13 other countries.
Product
ConMed Anchor Tissue Retrieval System", 12 MM, 300 ML (5/BX) Catalog Number: TRS-ROBO-12 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1282-2019·2019-05-15
Medtronic Guardian Connect App Recalled for Silent Operating System Shutdowns
Medtronic is recalling the Guardian Connect App because the operating system may close it without warning, preventing users from receiving critical blood glucose alerts.
Product
Guardian Connect App CSS7200 used on the iPhone, iPad, and iPod Touch devices.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1304-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise sterility. The recall covers units distributed worldwide.
Product
ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1306-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Sterility Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall covers 5,034 units distributed worldwide.
Product
ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:TRS190SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1303-2019·2019-05-15
Zimmer Biomet Recalls T7 Driver Solid AO Due to Fracture Risk
Zimmer Biomet is recalling 1,924 T7 Driver Solid AO units because they may fracture, bend, or shear during use.
Product
T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1285-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Goggles Due to Latex Mislabeling
Cardinal Health is recalling ChemoPlus Protective Wrap-around Goggles because the kit labels state they are latex-free, but the goggle straps contain natural rubber latex.
Product
ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1286-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Chemo Spill Kits Due to Latex
Cardinal Health 200, LLC is recalling ChemoPlus Chemo Spill Kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.
Product
ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise the sterility of the product.
Product
ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1216-2019·2019-05-15
Alpha Omega Engineering Recalls Neuro Omega Systems Due to Tissue Harm Risk
Alpha Omega Engineering is recalling 29 Neuro Omega Systems because improperly connected cables may cause high charge density, leading to tissue harm.
Product
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and display bioelectric signals, and stimulate nerves and brain tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling the Anchor Tissue Retrieval System due to seal defects that may compromise sterility.
Product
ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1250-2019·2019-05-08
Philips Fetal Spiral Electrode Recall Due to Metal Tip Breakage Risk
Philips is recalling Fetal Spiral Electrodes because the metal tip may break off and remain in a newborn's scalp during delivery.
Product
Fetal Spiral Electrode, Model No. 9898 031 37631
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1248-2019·2019-05-08
Baxter SIGMA Spectrum Infusion Pumps Recalled for Flow Rate Testing Errors
Baxter Healthcare is recalling 158 SIGMA Spectrum Infusion Pumps because flow rate tests were performed for less than the required time, potentially leading to inaccurate fluid administration.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The Baxter SIGMA Spectrum Infusion Pump with Master Drug Library is intended to be used for the controlled administration of fluids. These fluids may include…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1249-2019·2019-05-08
Roche Recalls cobas e 801 Immunoassay Analyzers Due to Signal Drops
Roche Diagnostics is recalling 149 cobas e 801 immunoassay analyzers because signal drops after bottle changeovers may lead to incorrect medical decisions.
Product
cobas e 801 immunoassay analyzer
Category
Medical Device
Distribution
31 states
SevereFDA (Devices)·Z-1226-2019·2019-05-08
DePuy Spine Recalls Concorde Lift Spinal Fusion Implants Due to Migration
DePuy Spine is recalling Concorde Lift spinal fusion implants because a complaint trend was observed for post-operative loss of height and migration.
Product
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)
Category
Medical Device
Distribution
Distributed nationwide

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16026–16050 of 27500