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

22651–22675 of 40299

ModerateFDA (Devices)·Z-2994-2018·2018-09-19
Diagnostica Stago Recalls STA N¿oplastine¿ CI Reagents Due to Quality Control Issues
Diagnostica Stago is recalling STA N¿oplastine¿ CI in-vitro diagnostic kits because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Product
Diagnostica Stago STA N¿oplastine¿ CI, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. REF: 00666 The STA¿ - N¿oplastine¿ CI kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿, STA…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3033-2018·2018-09-19
SPS Sterilization Recalls Edwards Femoral Venous Cannula Due to Shelf Life Labeling Error
SPS Sterilization is recalling one unit of an Edwards Lifesciences Femoral Venous Cannula because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences Femoral Venous Cannula, 20F X 55CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3035-2018·2018-09-19
SPS Sterilization Recalls Boston Scientific Wallstent Due to Expiration Date Error
SPS Sterilization is recalling two Boston Scientific Wallstent devices because the expiration date on the label exceeds the validated shelf life.
Product
Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 12MM X 90MM | 75CM L, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3028-2018·2018-09-19
SPS Sterilization Recalls Edwards Lifesciences Aortic Cannula Due to Labeling Error
SPS Sterilization is recalling 6 units of Edwards Lifesciences EZ Glide Aortic Cannulas because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3018-2018·2018-09-19
Remel Thioglycollate Medium Recalled for Performance Testing Failures
Remel Inc is recalling specific lots of Thioglycollate Medium because the products intermittently failed performance testing during stability studies.
Product
remel THIOGLYCOLLATE MEDIUM W/O INDICATOR. W/ DEXTROSE (a) 9ML, REF 064700 (b) 10ML, REF 07176 (c) 9ML, REF 064702
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-3032-2018·2018-09-19
SPS Sterilization Recalls Edwards Femoral Venous Cannula Due to Shelf Life Error
SPS Sterilization is recalling one unit of an Edwards Lifesciences Femoral Venous Cannula because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3029-2018·2018-09-19
SPS Sterilization Recalls Resterilized Venous Drainage Cannulas Due to Shelf Life Labeling
SPS Sterilization is recalling 10 units of resterilized venous drainage cannulas because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 38FRX40CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3022-2018·2018-09-19
ev3 TurboHawk Peripheral Plaque Excision System Recall for Incompatible Accessories
Micro Therapeutics is recalling 67 units of the ev3 TurboHawk Peripheral Plaque Excision System because packaged accessories are incompatible with the catheter, potentially preventing the removal of excised material.
Product
ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIUM, Model THS-LX-C for peripheral vascular use.
Category
Medical Device
Distribution
10 states
ModerateFDA (Devices)·Z-3039-2018·2018-09-19
SPS Sterilization Recalls Resterilized Boston Scientific Wallstent RP Endoprosthesis
SPS Sterilization is recalling two units of resterilized Boston Scientific Wallstent RP Endoprosthesis because the labeling expiration date exceeds the validated shelf life.
Product
Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 8MM X 80MM | 75CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3031-2018·2018-09-19
SPS Sterilization Recalls Avid Venous Drainage Cannulas Due to Shelf Life Labeling
SPS Sterilization is recalling 5 units of Avid Dual Stage Venous Drainage Cannulas because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3042-2018·2018-09-19
LeMaitre AnastoClip GC Closure System Recalled for Incorrect Instructions
LeMaitre Vascular is recalling AnastoClip GC Closure Systems because the included instructions listed uses not cleared by the FDA.
Product
AnastoClip GC Closure System, REF# 4007-08 a closure system designed to penetrate the outer layers of tissue during the forming of an anastomosis or closing of a vessel with possible intraluminal penetration.
Category
Medical Device
Distribution
5 states
ModerateFDA (Devices)·Z-3036-2018·2018-09-19
SPS Sterilization Recalls Boston Scientific Wallstent Tracheobronchial Stents
SPS Sterilization is recalling two Boston Scientific Wallstent tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life of the sterilization process.
Product
Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 22MM X 45MM | 75CM L, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3038-2018·2018-09-19
SPS Sterilization Recalls Resterilized Boston Scientific Wallstent Enteral Endoprosthesis
SPS Sterilization, Inc. is recalling two units of resterilized Boston Scientific Wallstent Enteral Endoprosthesis because the expiration date on the labeling exceeds the validated shelf life.
Product
Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent, 22MM X 90MM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3041-2018·2018-09-19
SPS Sterilization Recalls Venture Rx Catheters Due to Shelf Life Labeling Error
SPS Sterilization is recalling 3 resterilized Venture Rx Catheters because the expiration date on the label exceeds the validated shelf life.
Product
Vascular Solutions Venture Rx Catheter, 6F, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-2993-2018·2018-09-19
Diagnostica Stago Recalls STA N¿oplastine¿ CI Plus Reagents Due to Quality Control Failures
Diagnostica Stago is recalling 24,043 kits of STA N¿oplastine¿ CI Plus reagents because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Product
Diagnostica Stago STA N¿oplastine¿ CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. (REF 00667) The STA¿ - N¿oplastine¿ CI Plus kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3040-2018·2018-09-19
SPS Sterilization Recalls Boston Scientific Wallstent RP Endoprosthesis Due to Labeling Error
SPS Sterilization, Inc. is recalling three Boston Scientific Wallstent RP Endoprosthesis tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life.
Product
Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding Stent, 10MM X 94MM | 135CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3026-2018·2018-09-19
Vascular Technology Recalls 10 Mislabeled 8 MHz Surgical Doppler Transceivers
Vascular Technology, Inc. is recalling 10 surgical Doppler transceivers that may be mislabeled as 20 MHz units instead of 8 MHz units.
Product
VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-3019-2018·2018-09-19
Remel Thioglycollate Medium Recalled for Performance Testing Failures
Remel Inc is recalling Remel Thioglycollate Medium (Ref 05152) because products intermittently failed performance testing during stability studies.
Product
remel THIOGLYCOLLATE MEDIUM, REF 05152
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-3027-2018·2018-09-19
SPS Sterilization Recalls Resterilized Aortic Perfusion Cannulas Due to Shelf Life Labeling
SPS Sterilization, Inc. is recalling 10 units of resterilized Edwards Lifesciences Aortic Perfusion Cannulas because the expiration date on the labeling exceeds the validated shelf life.
Product
Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3037-2018·2018-09-19
Recall of Boston Scientific Tracheobronchial Stents Due to Sterilization Labeling Error
SPS Sterilization, Inc. is recalling two Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stents because the expiration date on the labeling exceeds the validated shelf life.
Product
Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 24MM X 70MM | 75CM L, resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3030-2018·2018-09-19
SPS Sterilization Recalls Edwards Venous Drainage Cannulas Due to Labeling Error
SPS Sterilization is recalling five units of Edwards Lifesciences venous drainage cannulas because the expiration date on the label exceeds the validated shelf life.
Product
Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 34F (11.3MM) X 40CM (16"), resterilized.
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-3034-2018·2018-09-19
SPS Sterilization Recalls Resterilized Edwards Arterial Perfusion Cannula
SPS Sterilization is recalling one resterilized Edwards Lifesciences Optisite Arterial Perfusion Cannula because its expiration date exceeds the validated shelf life.
Product
Edwards Lifesciences Optisite Arterial Perfusion Cannula, 22F X 24CM, resterilized.
Category
Medical Device
Distribution
8 states
LowFDA (Devices)·Z-3043-2018·2018-09-19
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products Cl- Slides
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides in serum samples.
Product
VITROS Chemistry Products Cl- Slides, Product Code 844 5207 Product Usage: For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum and plasma using VITROS 250/350/5,1 FS and 4600 Chemistry Systems…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3044-2018·2018-09-19
Ortho-Clinical VITROS Chloride Slides Recalled for Interference Issues
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides.
Product
VITROS Chemistry Products Cl- Slides, Product Code 684 4471 Product Usage For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using VITROS 250/350/5,1 FS and 4600 Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2990-2018·2018-09-12
GE Vivid E7 Ultrasound System Recalled for Power Cord Shock Risk
GE Medical Systems is recalling Vivid E7 ultrasound systems because the power cord may break and expose electrical conductors, creating a risk of electric shock.
Product
GE Vivid E7 ultrasound system Product Usage: Vivid E7 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of Fetal/Obstetrics; Abdominal…
Category
Medical Device
Distribution
Distributed nationwide

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22651–22675 of 40299