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

20226–20250 of 27682

HighFDA (Devices)·Z-1206-2017·2017-02-22
Atrium Medical Recalls Maquet Ocean Water Seal Chest Drains
Atrium Medical Corporation is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after use.
Product
Maquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1210-2017·2017-02-22
Atrium Medical Recalls Maquet Express Dry Seal Suction OCEAN DRAIN Chest Drains
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction OCEAN DRAIN chest drains because the manual vent valve may fail to re-seal after use.
Product
Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE Reference: 2002-400 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1214-2017·2017-02-22
Siemens Recalls ONCOR Radiation Therapy Systems Due to Collimator and Weld Defects
Siemens is recalling 194 ONCOR radiation therapy systems in the US due to incorrect collimator position displays and improper weld seams.
Product
ONCOR Impression, ONCOR Impression plus, and ONCOR Expression Medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1191-2017·2017-02-22
Encore Medical Recalls LIMA Modular Revision Hip Stems Due to Sterilization Error
Encore Medical is recalling 13 LIMA Modular Revision Hip Stems because they were inadvertently re-sterilized, which may compromise the integrity of the safety screw.
Product
LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of a modular stem coupled with a proper neck by means of a Morse taper stabilized during the implantation phase by a safety screw. This system is particularly…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1195-2017·2017-02-22
Argon Medical Devices Recalls T-LOK Bone Marrow Biopsy Needles
Argon Medical Devices is recalling T-LOK bone marrow biopsy needles due to a potential defect in the blister packaging that may compromise sterility.
Product
T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 EXT CAN Intended for the purpose of harvesting bone and/or bone marrow specimens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2017·2017-02-22
Abbott StarClose SE Vascular Closure System Recall for Deployment Failure
Abbott Vascular is recalling the StarClose SE Vascular Closure System because the device may fail to deploy the clip.
Product
StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1197-2017·2017-02-22
Advanced Sterilization Products Recalls STERRAD NX Sterilization Systems
Advanced Sterilization Products is recalling STERRAD NX Sterilization Systems because the door interlock may disengage for 20 seconds after a power outage.
Product
STERRAD NX Sterilization System, Product Code: 10033, 10033-002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1209-2017·2017-02-22
Atrium Medical Recalls Maquet Express Dry Seal Suction Chest Drains
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction chest drains because the manual vent valve may fail to re-seal after being depressed.
Product
Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE W/S Reference: 2002-300 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2017·2017-02-22
Merge Healthcare Recalls Schiller PB 1000 Blood Pressure Pumps
Merge Healthcare is recalling Schiller PB 1000 blood pressure pumps because insufficient voltage causes them to fail before reaching adequate pressure.
Product
The Schiller PB 1000, also known as: Merge Hemo Patient Data Module (PDM), V2 model, a major component of the Merge Hemo software.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1205-2017·2017-02-22
Atrium Medical Recalls Maquet Ocean Water Seal Chest Drains
Atrium Medical is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after being depressed.
Product
Maquet Ocean Water Seal Chest Drain, Single Collection WAC Reference: 2002-000 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1207-2017·2017-02-22
Atrium Medical Recalls Maquet Oasis Chest Drains Due to Valve Defect
Atrium Medical is recalling Maquet Oasis chest drains because the manual vent valve may fail to re-seal after use.
Product
Maquet Oasis Dry Suction Water Seal Chest Drain, Single Collection w/AC Reference: 3600-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1211-2017·2017-02-22
Atrium Medical Recalls Maquet Express Dry Seal Suction OASIS Drain
Atrium Medical Corporation is recalling 18 units of Maquet Express Dry Seal Suction OASIS Drain because the manual vent valve may fail to re-seal.
Product
Maquet Express Dry Seal Suction OASIS DRAIN, DRY PEDI W/AC Reference: 3612-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2017·2017-02-22
Siemens ARTISTE MV System Recalled for Collimator and Weld Defects
Siemens is recalling 194 ARTISTE MV radiation therapy systems due to incorrect collimator position displays and improper weld seams.
Product
ARTISTE MV System, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1199-2017·2017-02-22
Acumed Recalls 6-Hole Pubic Symphysis Plates Due to Material Error
Acumed LLC is recalling 15 units of 6-hole Pubic Symphysis plates because they were manufactured with the wrong titanium alloy.
Product
6-hole Pubic Symphysis plate (PN 70-0451). The pelvic bone plates for the pelvic ring are a series of plates with varying lengths that function as internal fixation devices for fractures, fusions and osteotomies of the pelvic ring. The plates are strategically pre-contoured…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1208-2017·2017-02-22
Atrium Medical Recalls Maquet Express Dry Seal Suction Chest Drains
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction Chest Drains because the manual vent valve may fail to re-seal after being depressed.
Product
Maquet Express Dry Seal Suction Chest Drain, Single Collection w/AC Reference: 4000-100N Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1213-2017·2017-02-22
Siemens Oncor Avant-garde Radiation Therapy Systems Recalled for Sensor Defects
Siemens is recalling 194 Oncor Avant-garde radiation therapy systems due to incorrect collimator position displays and improper weld seams.
Product
ONCOR Avant-garde, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1183-2017·2017-02-15
Invacare Recalls Bariatric Beds Due to Fire Hazard
Invacare is recalling Bariatric Beds (BARPKG-IVC 1633) because a quality issue with the junction box may cause sparks and result in a fire.
Product
Bariatric Bed - BARPKG-IVC 1633
Category
Medical Device
Distribution
37 states
SevereFDA (Devices)·Z-1185-2017·2017-02-15
Invacare Bariatric Bed Junction Box Recalled for Fire Risk
Invacare is recalling 161 bariatric bed junction boxes due to a quality issue that may cause sparks and result in a fire.
Product
Junction Box - 1104343 and 1193560
Category
Medical Device
Distribution
37 states
SevereFDA (Devices)·Z-1182-2017·2017-02-15
Invacare Bariatric Bed Recall Due to Fire Hazard
Invacare is recalling 411 bariatric beds because the junction box may emit sparks and cause a fire.
Product
Bariatric Bed - BAR600IVC
Category
Medical Device
Distribution
37 states
SevereFDA (Devices)·Z-1184-2017·2017-02-15
Invacare Recalls Bariatric Bed Foot Sections Due to Fire Risk
Invacare Corporation is recalling 292 bariatric bed foot sections because a quality issue with the junction box may cause sparks and result in a fire.
Product
Foot Section - BAR5490IVC
Category
Medical Device
Distribution
37 states
SevereFDA (Devices)·Z-1138-2017·2017-02-15
Carestream DRX-Revolution Mobile X-Ray System Recalled for Brake Failure
Carestream Health is recalling DRX-Revolution Mobile X-Ray Systems because a complaint alleged the unit could not be stopped when applying the brake, resulting in a crash into an elevator.
Product
Carestream DRX-Revolution Mobile X-Ray System, Model DRXR-1, Catalog No. 1019397 (all other countries), Catalog No. 1060177 (China only) -- Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1137-2017·2017-02-15
AngioDynamics Recalls Celerity ECG Cable Accessory Packs Due to Soldering Defect
AngioDynamics is recalling Celerity ECG Cable Accessory Packs because the ECG clip cable may not be soldered correctly, potentially preventing the device from conducting ECG signals.
Product
Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labels: (a) angiodynamics UPN/Product No. H787471431, REF/Catalog No. 47-143 -- Legal Manufacturer: AngioDynamics, Inc. 10 Glens Falls Technical Park, Glens Falls, NY 12801; and (b) medCOMP…
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-0927-2017·2017-02-15
Bayer Recalls Medrad Intego PET Infusion System Pumps
Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.
Product
MEDRAD Intego PET Infusion System - Pump Intended to deliver accurate doses of Fluoredeoxyglucose or F-Sodium Fluoride and commonly used flushing solutions to patients during molecular imaging (nuclear medicine) diagnostic procedures. It is also intended to provide effective…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1178-2017·2017-02-15
Boston Scientific Recalls EMBLEM S-ICD Programmer Model 3200
Boston Scientific is recalling 4,500 EMBLEM S-ICD Programmer Model 3200 units due to a potential risk of radio frequency interference causing unintended commands during in-clinic sessions.
Product
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1144-2017·2017-02-15
Physio-Control Recalls LIFEPAK 15 Defibrillators with Erroneous CO2 Readings
Physio-Control is recalling LIFEPAK 15 Monitor/Defibrillators with End-Tidal CO2 options because the CO2 reading may intermittently display an incorrect value of XXX.
Product
LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions.
Category
Medical Device
Distribution
Distributed nationwide

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20226–20250 of 27682