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

18401–18425 of 40124

HighFDA (Devices)·Z-1048-2020·2020-02-12
Centurion Medical Products Recalls Sterile Surgical Trays Due to Seal Defects
Centurion Medical Products is recalling various sterile surgical trays and packs because incomplete seals may compromise sterility.
Product
Centurion-_General Surgery Trays DYNDA1127A RADIOLOGY CUT DOWN TRAY #1 DYNDA1178 ICIO TRAY DYNDA1183 AUXILARY TOWEL PACK DYNDA1223 CUSTOM PREP CUP KIT DYNDA1223 CUSTOM PREP CUP KIT DYNDA1246A CIRCUMCISION PACK DYNDA1349A CIRCUMCISION TRAY DYNDA1388 STERILE EK DOUBLE PACK…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1051-2020·2020-02-12
Centurion Circumcision Tray Kits Recalled for Incomplete Sterile Seals
Centurion Medical Products is recalling specific Circumcision Tray Kits because incomplete seals on the sterile packaging may compromise sterility.
Product
Centurion- Circumcision Tray Kits DYNDF1078C CIRCUMCISION TRAY DYNDF1082 CIRCUMCISION TRAY DYNDF1082 CIRCUMCISION TRAY DYNDF1093C UNIVERSAL CIRCUMCISION TRAY W/O CLAMP DYNDF1093C UNIVERSAL CIRCUMCISION TRAY W/O CLAMP DYNDF1109 TRAY,CIRCUMCISION DYNDF1128…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2020·2020-02-12
Centurion Medical Products Recalls Dressing Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific dressing trays and medical packs because incomplete seals may compromise sterility.
Product
Centurion- Dressing Tray M101156A DRESSING TRAY M101167A DRESSING TRAY M101168A DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101170A MAJOR DRESSING TRAY M101172B MINOR CORE DRESSING TRAY M101172B MINOR CORE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1056-2020·2020-02-12
Centurion Medical Products Recalls Sterile Biopsy and Arthrogram Trays
Centurion Medical Products is recalling specific sterile biopsy and arthrogram trays due to incomplete seals that may compromise sterility.
Product
Centurion- SPEC0002B ARTHROGRAM TRAY SPEC0002B ARTHROGRAM TRAY SPEC0004C ARTHROGRAM TRAY SPEC0071B CUSTOM BX TRAY SPEC0076G STEREO BIOPSY PACK-LF SPEC0122 BASIC BIOPSY TRAY SPEC0130B BREAST BIOPSY TRAY SPEC0158A CT BIOPSY TRAY SPEC0248B GENERAL BIOPSY TRAY- LF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2020·2020-02-12
Ethicon Recalls VICRYL Sutures Due to Braid Fraying
Ethicon is recalling specific VICRYL sutures because braid fraying may reduce tensile strength. The recall covers 23,688 units distributed in the US and Puerto Rico.
Product
Coated VICRYL (Polyglactin 910) Suture, 18" (45cm) Product Code J497H. The device is a synthetic absorbable sterile surgical suture.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1021-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NONREINF SURG GOWN 3XL BNS, Item Code 9585N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0960-2020·2020-02-12
Cook Inc. Recalls Fixed Core Straight Safety Wire Guide
Cook Inc. is recalling 15 units of Fixed Core Straight Safety Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients.
Product
Fixed Core Straight Safety Wire Guide, Guidewire, Global Product Number G14285
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0969-2020·2020-02-12
Cook Percutaneous Pigtail Nephrostomy Set Recalled for Wire Guide Loading Error
Cook Inc. is recalling Percutaneous Pigtail Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
Product
Percutaneous Pigtail Nephrostomy Set , Global Product No. G14094 G14095 G14899 G14329
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1081-2020·2020-02-12
Centurion Debridement Tray Recalled for Incomplete Sterile Package Seals
Centurion Medical Products Corporation is recalling Debridement Trays because incomplete seals on the sterile package may compromise sterility.
Product
Centurion- I86625 DEBRIDEMENT TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1074-2020·2020-02-12
Centurion Skin Prep Tray Recalled for Incomplete Sterile Package Seals
Centurion Medical Products Corporation is recalling Skin Prep Trays due to incomplete seals on the sterile package, which may compromise sterility.
Product
Centurion-Skin Prep Tray DYNDP1015 SKIN PREP TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2020·2020-02-12
Centurion Medical Recalls Skin Prep Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific lots of sterile skin prep trays because incomplete seals may compromise sterility.
Product
Centurion-Skin Prep Trays SP1180 DRY PREP SET SP200 SKIN SCRUB TRAY SP415 STERILE GAUZE SPONGE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1005-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABREINF SCRUB SURG GWN L NS, Gown. Item Code 90970NA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1094-2020·2020-02-12
Centurion Medical Recalls Umbilical Catheter Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific umbilical catheter trays because incomplete seals on the sterile package may compromise sterility.
Product
Centurion- UVT1045 UMBILICAL ARTERY TRAY UVT1055 UVC KIT UVT1065 UMBILICAL VESSEL CATHETER TRAY UVT170 UMBILICAL VESSEL TRAY W/O CATHETER UVT280 UMBILICAL ARTERY TRAY UVT460 UMBILICAL CATHETER TRAY UVT505 UMBILICAL VESSEL CATH INSERT TR W/O CATH UVT630…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0965-2020·2020-02-12
Cook Inc. Recalls Angled Tip Ureteral Catheter Sets Due to Loading Defect
Cook Inc. is recalling 13,388 Angled Tip Ureteral Catheter Sets because the wire guide may load incorrectly, causing the stiff tip to enter the patient instead of the flexible tip.
Product
Angled Tip Ureteral Catheter Set, Ureteral Catheter, Global Product No. G14598
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1041-2020·2020-02-12
Implant Direct Sybron Recalls Legacy 3 Dental Implants Due to Incorrect Packaging
Implant Direct Sybron is recalling 72 Legacy 3 dental implants because some packages contain incorrect implants, which could lead to surgery rescheduling.
Product
Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0981-2020·2020-02-12
Pacific Medical Ultrasound Transducers Recalled for Lack of FDA Clearance
Pacific Medical Group Inc. is recalling GE Corometrics Nautilus Ultrasound Transducers because they were distributed before receiving required FDA 510(k) and international clearances.
Product
Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob, 5700HAX, FFCM5205
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-0990-2020·2020-02-12
Cardinal Health Recalls Genius 2 Tympanic Thermometers for Accuracy Drift
Cardinal Health is recalling Genius 2 Tympanic Thermometers because calibration frequency may not ensure readings stay within the stated accuracy range.
Product
Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1105-2020·2020-02-12
Intuitive Surgical Recalls Da Vinci Xi EndoWrist Monopolar Curved Scissors
Intuitive Surgical is recalling 286 Da Vinci Xi EndoWrist Monopolar Curved Scissors because they are not recognized by the integrated electrosurgical unit, preventing the activation of monopolar energy.
Product
Da Vinci Xi/X EndoWrist Monopolar Curved scissors (MCS), model number 470179-19, UDI: (00) 886874112298
Category
Medical Device
Distribution
37 states
ModerateFDA (Devices)·Z-0931-2020·2020-02-12
PediaLift Access Device Recalled for Labeling Compliance Issues
PediaLift LLC is recalling 11 PediaLift Access Devices because the firm could not obtain a satisfactory Certificate of Conformance from the original vendor regarding labeling requirements.
Product
PediaLift Access Device, Device Identifier: B751PDLFT0
Category
Medical Device
Distribution
5 states
ModerateFDA (Devices)·Z-0994-2020·2020-02-12
Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift
Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.
Product
Genius 2 Tympanic Thermometer Private Label Item Code: 3069
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1102-2020·2020-02-12
Wright Medical Recalls EVOLVE Modular Radial Heads Due to Sizing Errors
Wright Medical Technology is recalling two lots of EVOLVE Modular Radial Heads because the product size in the package may be incorrect. Both labels and laser markings are wrong.
Product
WRIGHT EVOLVE Proline Head, Size: +2, OD: 22mm, REF 496H222
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-0982-2020·2020-02-12
Pacific Medical Nautilus Ultrasound Recalled for Missing Clearances
Pacific Medical Group Inc. is recalling GE Corometrics Nautilus Ultrasound units because fetal transducers were distributed before receiving required FDA and international clearances.
Product
Pacific Medical GE Corometrics Nautilus Ultrasound, 5700 (Old Style), FFCM5660
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-0992-2020·2020-02-12
Cardinal Health Genius 2 Tympanic Thermometer Recall for Accuracy Drift
Cardinal Health is recalling Genius 2 tympanic thermometers because readings may drift upward over time, potentially exceeding the stated accuracy range.
Product
Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0984-2020·2020-02-12
Pacific Medical Fetal Transducers Recalled for Missing Regulatory Clearances
Pacific Medical Group Inc. is recalling 261 fetal transducers distributed in the U.S. and abroad before receiving required FDA and international clearances.
Product
Pacific Medical Philips M1355A Toco Transducer with belt wire/knob, FFPH3250
Category
Medical Device
Distribution
45 states
ModerateFDA (Devices)·Z-0979-2020·2020-02-12
Pacific Medical fetal transducers recalled for lack of regulatory clearance
Pacific Medical Group is recalling 772 fetal transducers distributed in the U.S. and abroad before receiving required FDA 510(k) and international clearances.
Product
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Category
Medical Device
Distribution
45 states

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18401–18425 of 40124