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

32176–32200 of 40325

ModerateFDA (Devices)·Z-2473-2015·2015-09-02
Baxter MiniCap Extended Life PD Transfer Set Labeling Recall
Baxter Healthcare Corp. is recalling 33,474 units of MiniCap Extended Life PD Transfer Sets to update labeling with additional safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnections are performed at the transfer…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2468-2015·2015-09-02
Stryker recalls mislabeled 5mm trocar sleeves due to length discrepancy
Stryker Sustainability Solutions is recalling 90 reprocessed trocar sleeves labeled as 100mm but containing 75mm models.
Product
Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery, Inc. Excel Trocar Sleeve w/Stability Sleeve 5mm x 100mm Reprocessed by Stryker Sustainability Solutions Product Usage: The Reprocessed Ethicon ENDOPATH¿ XCEL Universal Trocar Stability Sleeve is a sterile…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2448-2015·2015-09-02
Alcon Recalls LX3 Microscope Floor Stands Due to Cabling Issues
Alcon is voluntarily recalling LX3 Microscope Floor Stands because cabling issues may cause loss of functionality or illumination failure.
Product
LX3 Floor Stand for Endure Luxite Envision Optical System; Endure LuxOR Q-Vue. Product Usage: The LX3 Microscope Floor Stand is an accessory to the LuxOR Opthalmic Microscope and the LuxOR Opthalmic Microscope with Q-VUE 3-D Assistant Visualization and provides a portable…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2471-2015·2015-09-02
Baxter Recalls MiniCap Peritoneal Dialysis Transfer Sets for Labeling Updates
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets to update labeling with new safety instructions and warnings.
Product
MiniCap Extended Life PD Transfer Set Extra Short (4") with Twist Clamp. Product Code: 5C4483. intended for use with Baxter Locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2476-2015·2015-09-02
AMUSA Recalls 0.9% Sodium Chloride Injection Due to Process Control Issues
MRP, LLC dba AMUSA is recalling 0.9% Sodium Chloride Injection because procedures for product acceptance and control were not adequately established.
Product
0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
Category
Medical Device
Distribution
10 states
CriticalFDA (Devices)·Z-2367-2015·2015-08-26
Teleflex Medical Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes
Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.
Product
HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Left sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2372-2015·2015-08-26
Elite Biomedical Recalls Alaris Medley LVP Bezel Assemblies
Elite Biomedical Solutions LLC is recalling 346 Alaris Medley LVP Bezel Assemblies used in infusion pumps due to a risk of administering inappropriate fluid quantities.
Product
Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2329-2015·2015-08-26
FDA Recalls 657 Puritan Bennett 980 Ventilators Due to Volume Defects
The FDA is recalling 657 Puritan Bennett 980 Ventilators because tidal volumes may be lower than set in neonatal mode, potentially causing respiratory compromise.
Product
Puritan Bennett 980 Ventilator System, Universal (with neonatal functionality enabled) and Neonatal Models. Designed for use on Neonatal (NICU) through Adult patient populations who require respiratory support or mechanical ventilation and weigh a minimum of 0.3 kg (0.66 lb).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2343-2015·2015-08-26
Draeger Evita Infinity V500 Ventilator Battery Recall
Draeger Medical is recalling 2,081 Evita Infinity V500 ventilators because the optional PS500 battery capacity did not last as long as expected.
Product
PS500 of an IACS Workstation Critical Care (Evita Infinity V500); intended for the ventilation of adult, pediatric and neonatal patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2437-2015·2015-08-26
Siemens Intevo Series Imaging Systems Recalled for Overheating Risk
Siemens Medical Solutions USA is recalling 185 Intevo Series imaging systems because improper fuses could cause the Power Controller assembly to overheat.
Product
Siemens Intevo Series system, a radiological imaging system that is a combination of a single photon emission computed tomography (SPECT) camera system for nuclear medicine images, and a computed tomography (CT) camera system for x-ray images.
Category
Medical Device
Distribution
51 states
SevereFDA (Devices)·Z-2371-2015·2015-08-26
Elite Biomedical Recalls Alaris Medley LVP Frame Membranes
Elite Biomedical Solutions LLC is recalling 609 Alaris Medley LVP Frame Membranes because the defect could allow fluid intrusion, potentially leading to injury or death.
Product
Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2362-2015·2015-08-26
CareFusion Alaris Syringe Pump Recall for Unresponsive Control Defect
CareFusion 303, Inc. is recalling Alaris Syringe Pumps, Model 8110, because they may become unresponsive to key presses after a channel error is cleared.
Product
Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2369-2015·2015-08-26
Teleflex Sheridan SHER-I Bronch Accessory Pack Recalled for Connector Defect
Teleflex Medical is recalling Sheridan SHER-I Bronch Accessory Packs because the double swivel connector may crack or separate on the endobronchial tube.
Product
HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a patient's upper airway.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2368-2015·2015-08-26
Teleflex Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes Due to Connector Cracking
Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.
Product
HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2433-2015·2015-08-26
Medline Electrical Surgical Clippers Recalled for Overheating Charging Base
Medline is recalling 7,602 electrical surgical clippers because the charging base can overheat and smoke. The units were distributed in the U.S. and eight other countries.
Product
Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended for the removal of body hair from patients as required prior to surgery or other minor procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2370-2015·2015-08-26
Teleflex Medical Recalls Sheridan Double Swivel Connectors Due to Cracking Risk
Teleflex Medical is recalling Sheridan double swivel connectors because they may crack or separate on endobronchial tubes.
Product
HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2394-2015·2015-08-26
Winco Care Cliner Chairs Recalled for Non-Fire-Retardant Foam
Winco Mfg. is recalling four Care Cliner X-Large chairs because the foam used was standard foam rather than fire-retardant foam.
Product
Winco Care Cliner X-Large - with Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2393-2015·2015-08-26
Winco Care Cliner X-Large Chair Recalled for Fire Retardant Foam Mislabeling
Winco Mfg., LLC is recalling Care Cliner X-Large chairs because the foam was mislabeled as fire retardant but is actually standard foam.
Product
Winco Care Cliner X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2392-2015·2015-08-26
Winco Care Cliner Standart Steel Casters Recalled for Fire Hazard
Winco Mfg., LLC is recalling Care Cliner Standart chairs because the foam used was not fire retardant as required.
Product
Winco Care Cliner Standart - Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2206-2015·2015-08-26
American Science & Engineering Recalls Gemini Cabinet X-ray Systems
American Science & Engineering is recalling 125 Gemini Cabinet X-ray systems because a fault may cause X-rays to be produced without the indicator lights illuminating.
Product
American Science & Engineering Inc,Gemini Cabinet X-ray system.
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-2400-2015·2015-08-26
Winco Elite Care Chairs Recalled for Fire Retardant Foam Mislabeling
Winco Mfg. is recalling 32 Elite Care chairs because foam shipped as fire retardant was actually standard foam, failing safety standards.
Product
Winco Elite Care Cliner w/Swing Away Arms Standard - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2410-2015·2015-08-26
Teleflex Recalls Bronchial One Lumen Tubes Due to Connector Detachment
Teleflex is recalling Bronchial One Lumen Tubes because the cobb connector may detach from the main connector prior to use.
Product
Bronchial One Lumen Tube - Right
Category
Medical Device
Distribution
40 states
HighFDA (Devices)·Z-2397-2015·2015-08-26
Winco Drop Arm Care Cliner Chairs Recalled for Fire Hazard
Winco Mfg. is recalling three Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.
Product
Winco Drop Arm Care Cliner X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2398-2015·2015-08-26
Winco Designer Care Cliner chairs recalled for non-compliant foam
Winco Mfg., LLC is recalling two Designer Care Cliner chairs because the foam used was not fire retardant as required.
Product
Winco Designer Care Cliner - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2403-2015·2015-08-26
Winco Patient Recliner Recalled for Non-Fire-Retardant Foam
Winco Mfg. is recalling specific patient recliners because the foam used was standard foam rather than fire-retardant foam, failing to meet safety standards.
Product
Winco Nocturnal Elite Care Cliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)
Category
Medical Device
Distribution
Distributed nationwide

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32176–32200 of 40325