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

31101–31125 of 40449

HighFDA (Devices)·Z-0789-2016·2016-02-17
Richard Wolf Reusable Rotary Blade Recall Due to Weak Welds
Richard Wolf Medical Instruments Corp. is recalling ten reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.
Product
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0688-2016·2016-02-17
Moog Recalls Curlin Infusion Pumps Due to Calibration Defect
Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.
Product
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0787-2016·2016-02-17
DePuy SIGMA HP MBT Non-Keel Punch Knee Instrument Recalled
DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.
Product
SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0759-2016·2016-02-17
Trumpf Medical Systems Recalls Patient Transport Shuttles Due to Tilting Hazard
Trumpf Medical Systems is recalling 1,284 patient transport shuttles because the table top may tilt down quickly in the maximum Trendelenburg position.
Product
Patient transport Shuttle with Trendelenburg quick adjustment function (Jupiter, Mars, Titan, TruSystem and Saturn operating table systems). The shuttle is intended for the following applications: 1. Transfer, transport and storage of exchangeable table tops in the Trumpf…
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0768-2016·2016-02-17
GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.
Product
GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0769-2016·2016-02-17
GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.
Product
GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0792-2016·2016-02-17
Mizuho OSI Trios Table Base Recall for Missing Retaining Ring
Mizuho OSI is recalling 33 Trios table bases because a missing retaining ring may cause the clutch to jam, preventing patient rotation.
Product
Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0790-2016·2016-02-17
Richard Wolf Reusable Rotary Blade Recalled for Weak Welds
Richard Wolf Medical Instruments Corp. is recalling four reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.
Product
Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0788-2016·2016-02-17
Zimmer Biomet Recalls Endobon Xenograft Granules Due to Cytotoxicity Failure
Biomet France SARL is recalling Endobon-Xenograft Granules because the product failed cytotoxicity tests at 36 months. Use past the 18-month shelf life may cause patient illness or injury.
Product
Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge…
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0770-2016·2016-02-17
GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure
GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.
Product
GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
Category
Medical Device
Distribution
4 states
HighFDA (Devices)·Z-0764-2016·2016-02-17
Philips Allura Xper FD20 Ceiling Version Recalled for C-Arc Movement
Philips is recalling 15 Allura Xper FD20 Ceiling version units because improper adjustment may cause the C-arc to continue moving after stopping.
Product
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0791-2016·2016-02-17
Richard Wolf Reusable Rotary Blade Recalled for Weak Welds
Richard Wolf Medical Instruments Corp. is recalling two reusable rotary blades due to weak welds that may cause the product to break during surgical use.
Product
Reuseable rotary blade/abrader, product number 899751514. The oval burr frontally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0771-2016·2016-02-17
Accuray CyberKnife Robotic Recall for Potential Gun Box Mounting Bracket Failure
Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.
Product
CyberKnife Robotic; Catalog/part number 032000 and 033000 Cosmetic cover package. Product Usage: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors, and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0761-2016·2016-02-17
Del Medical VS200 Radiographic Cassette Holder Recall for Falling Hazard
Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.
Product
VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0763-2016·2016-02-17
GE Medical Systems Recalls Mavig Monitor Suspension System Due to Fall Risk
GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.
Product
Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2016·2016-02-17
Del Medical VS300 Radiographic Cassette Holder Recall for Falling Hazard
Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.
Product
VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0778-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Safety Information in Instructions
Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.
Product
IMPLANT,TM, MTX FULL 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMT4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0783-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMTB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0773-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMM4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0785-2016·2016-02-17
Bard Distaflo Vascular Bypass Graft Recalled for Size Mislabeling
Bard Peripheral Vascular Inc is recalling four units of Bard Distaflo Vascular Bypass Grafts due to size mislabeling. The 8 mm grafts are incorrectly labeled as 6 mm.
Product
Bard Distaflo Vascular Bypass Graft; Product Code: DF6006SC; 8 mm x 60 cm. Intended for bypass or reconstruction of peripheral arterial blood vessels.
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-0781-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal implants because safety information was omitted from the instructions for use.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMTB10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0752-2016·2016-02-17
Toshiba INFX-8000V X-Ray System Recalled for Dose Meter Error
Toshiba is recalling four INFX-8000V Bi-Plane X-Ray Interventional Systems because a software error caused dose data to be lost during specific imaging procedures.
Product
INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0796-2016·2016-02-17
Salter Labs Recalls T-piece Nebulizers Due to Fit Issues
Salter Labs is recalling 70 T-piece Nebulizers because the T-piece does not fit on the nebulizer. The devices were distributed in six US states and China.
Product
T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-0772-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Instructions
Zimmer Dental Inc. is recalling specific dental implants because the latest instructions omitted information for certain models.
Product
IMPLANT,TM, MTX 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMM4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0774-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions
Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.
Product
IMPLANT,TM, MTX 4.1 mm x 13 mm diameter 3.5 mm Catalog #TMM4B13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide

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31101–31125 of 40449