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

19776–19800 of 27647

HighFDA (Devices)·Z-1741-2017·2017-04-12
Recall of Sterile Eye Pads Due to Compromised Sterility Barrier
Covidien is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility. The recall affects units distributed worldwide.
Product
Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. It is supplied sterile to allow for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1731-2017·2017-04-12
Centurion Ophthalmic Dressing Kits Recalled for Sterile Packaging Breach
Centurion Medical Products is recalling 210 ophthalmic dressing kits due to a potential breach in the sterile packaging of the included eye pads.
Product
OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1751-2017·2017-04-12
Philips BrightView XCT Gamma Cameras Recalled for Brake Hub Assembly Error
Philips is recalling 90 BrightView XCT gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView XCT model number 882482 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated, and…
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1730-2017·2017-04-12
Centurion Medical Recalls Post-Op Eye Trays Due to Sterile Packaging Breach
Centurion Medical Products is recalling 476 Post-Op Eye Trays because the sterile eye pads inside may have had a packaging breach.
Product
POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1735-2017·2017-04-12
Centurion Convenience Kits Recalled Due to Potential Sterile Packaging Breach
Centurion Medical Products is recalling 1,692 Convenience Kits containing eye pads due to a potential breach in sterile packaging.
Product
OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1743-2017·2017-04-12
Sterile Saline Dressing Recalled Due to Compromised Sterility Barrier
FDA is recalling Kerlix Super Sponge Saline Dressings because the sterile barrier is breached, potentially compromising sterility.
Product
Covidien Kerlix Super Sponge Saline Dressing, Sterile Item Code: 3338 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic debridement process.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1732-2017·2017-04-12
Centurion Convenience Kits Recalled for Potential Sterile Packaging Breach
Centurion Medical Products is recalling 588 Convenience Kits containing Curity Oval Eye Pads due to a potential breach in sterile packaging.
Product
OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1750-2017·2017-04-12
Philips Recalls 84 BrightView SPECT Gamma Cameras Due to Brake Hub Defect
Philips is recalling 84 BrightView SPECT gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1742-2017·2017-04-12
Recall of Sterile Wound Dressings Due to Compromised Sterility Barrier
Covidien is recalling Curity Wet Dressings because the sterile barrier was breached, potentially compromising sterility. The recall affects units distributed worldwide.
Product
Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm), Sterile Item Code: 3337 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1746-2017·2017-04-12
BD Vacutainer Blood Collection Tubes Recalled for Stopper Pullout Risk
Becton Dickinson is recalling specific lots of BD Vacutainer Buffered Sodium Citrate blood collection tubes because stoppers may pull out during use.
Product
BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes, 4.5 mL, 13 x 75 mm, Mfd: Becton Dickinson and Company Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection Tube that provides means of collecting, transporting and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2017·2017-04-12
Recall of Sterile Eye Pads Due to Compromised Sterility Barrier
Covidien LLC is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility.
Product
Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7 cm), Sterile Item Code: 2841 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1734-2017·2017-04-12
Centurion Medical Recalls Post-Operative Ophthalmic Dressing Kits Due to Sterility Concerns
Centurion Medical Products is recalling 45 post-operative ophthalmic dressing kits because the eye pads inside may have had a breach in sterile packaging.
Product
POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
CriticalFDA (Devices)·Z-1417-2017·2017-04-05
Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Failure to Deliver Therapy
Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.
Product
HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1575-2017·2017-04-05
FDA Recalls 170 Sterile Laparoscopic Procedure Trays Due to Glove Splitting
Resource Optimization & Innovation LLC is recalling 170 sterile laparoscopic procedure trays because a light glove component can split during application, breaking the sterile field.
Product
Regard, Item Number: 880341003, Sterile, GS0775C - Laparoscopic - OSU
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1668-2017·2017-04-05
Resource Optimization Recalls Sterile Custom Procedure Trays Due to Glove Splitting
Resource Optimization & Innovation LLC is recalling 24 sterile custom procedure trays because a light glove component can split during application, breaking the sterile field.
Product
Regard, Item Number: 800508003, Sterile, LD0586C - C Section - Jasper
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1497-2017·2017-04-05
Merit Medical Recalls 7F Prelude Short Sheath Introducers Due to Detachment Risk
Merit Medical Systems is voluntarily recalling 1,265 units of 7F Prelude Short Sheath Introducers because the sheath marker tips may detach during use.
Product
7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070, K15-00170, PSS-7F-4-035MT, PSS-7F-4MT. Produc Usage: The Merit Prelude¿ Short Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1561-2017·2017-04-05
FDA Recalls Sterile Custom Procedure Trays Due to Glove Splitting Risk
Resource Optimization & Innovation LLC is recalling 42 sterile custom procedure trays because a light glove component can split, potentially breaking the sterile field.
Product
Regard, Item Number: 880323003, Sterile, LD0754C - C Section - OSU
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1646-2017·2017-04-05
FDA Recalls Sterile Custom Procedure Trays Due to Glove Splitting Hazard
Resource Optimization & Innovation LLC is recalling 274 sterile custom procedure trays because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800410004, Sterile, CV0479D- Open Heart PK - Spohn
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1580-2017·2017-04-05
Recall of Regard Open Heart Procedure Kits Due to Glove Splitting
Resource Optimization & Innovation LLC is recalling 117 sterile open heart procedure kits because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800410003, Sterile, CV0479C - Open Heart PK - Spohn
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1613-2017·2017-04-05
FDA Recalls 216 Custom Procedure Trays Due to Glove Splitting Hazard
Resource Optimization & Innovation LLC is recalling 216 custom procedure trays because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800553001, Sterile, OR0642A - Total Knee - Medical Center Santa Rosa
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1699-2017·2017-04-05
Stryker Visum LED Surgical Lighting System Recalled for Mounting Defect
Stryker is recalling 292 Visum LED Surgical Lighting systems because missing screws and user overloading may cause the equipment to fall.
Product
The Stryker Visum¿ LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light. Affected part numbers are 0682001432 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/FP), 0682001286 (EDS LIGHT SUSPENSION, CENTRAL AXIS…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1578-2017·2017-04-05
Recall of Regard Sterile Laparotomy Procedure Trays Due to Glove Defect
Resource Optimization & Innovation LLC is recalling 30 sterile laparotomy procedure trays because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 880342004, Sterile, GS0776D - Laparotomy - OSU
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1639-2017·2017-04-05
Recall of Regard Sterile Lap PK Spohn Custom Procedure Trays
Resource Optimization & Innovation LLC is recalling 3,000 sterile custom procedure trays because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800401002, Sterile, GS0470B - Lap PK - Spohn
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1656-2017·2017-04-05
Recall of Robotic Hysterectomy Kits Due to Light Glove Splitting
Resource Optimization & Innovation LLC is recalling 249 sterile robotic hysterectomy kits because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800416002, Sterile, GY0485B - Robotic Hysterectomy Pk - Spohn
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-1644-2017·2017-04-05
Recall of Regard Sterile Lap Chole Procedure Kits Due to Glove Defect
Resource Optimization & Innovation LLC is recalling 2,016 sterile lap chole procedure kits because a light glove component can split, breaking the sterile field.
Product
Regard, Item Number: 800409002, Sterile, GS0478B - Lap Chole PK - Spohn
Category
Medical Device
Distribution
2 states

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19776–19800 of 27647