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. 2,378 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,378 in last 12 months

Showing 2556125580 of 27,462 recalls

Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 10mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 2mm X 34cm Regular Tip with No Hole...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 3mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Regular Tip with No Holes...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 2mm X 32cm Regular Tip with 1 Hole Recalled...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Accuray Incorporated

Recalled Item: RoboCouch Patient Positioning System Product Usage: is intended for use...

The Issue: A5 gearboxes responsible for pitch (head up and head down) and roll (patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE Recalled by GE Healthcare, LLC Due to GE Healthcare has recently become...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice¿ Rayon Tipped OB/GYN Applicator Recalled by Owens & Minor...

The Issue: Owens & Minor Distribution, Inc. is conducting a market withdrawal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand RPM Respiratory Gating System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the RPM Respiratory Gating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE PET Discovery 610 Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...

The Issue: Stryker Orthopaedics received a report that a label on the external...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2013· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...

The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...

The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing