Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,908 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,908 in last 12 months

Showing 1186111880 of 27,462 recalls

Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...

The Issue: Space between the device and the packaging permits excessive movement which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...

The Issue: There may be a slightly protruding rivet on the distal end of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Bard Peripheral Vascular Inc

Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...

The Issue: Sterility compromised due to packaging pouches that may not be sealed properly

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...

The Issue: There may be a slightly protruding rivet on the distal end of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Avanos Medical, Inc.

Recalled Item: CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit Recalled by Avanos...

The Issue: The CORFLO PEG tube may become blocked at the center of the adapter...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test DNA Control-IVD for detection of DNA Recalled by...

The Issue: Extended Expiration Date prior to clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA Control- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter 6F Model 5540. For delivery of Recalled by...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Ion Torrent Dx No Template Control Kit- IVD for detection Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2020· Biomet, Inc.

Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...

The Issue: There were unknown bioburden levels prior to sterilization, which may affect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing