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. 2,471 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,471 in last 12 months

Showing 1694116960 of 27,462 recalls

Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Hologic, Inc

Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...

The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Ameditech Inc

Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...

The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...

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

Class III — Low RiskOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt HV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Beckman Coulter Inc.

Recalled Item: Coulter HmX CP and Coulter HmX AL Analyzers The purpose Recalled by Beckman...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt MV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Certified Safety Mfg Inc

Recalled Item: Burn Sheet Recalled by Certified Safety Mfg Inc Due to Burn Sheet has...

The Issue: Burn Sheet has possibility of being shredded.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt MV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...

The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Beckman Coulter Inc.

Recalled Item: Coulter LH 750 Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that additional clarification for the Blast...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Stryker Neurovascular

Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30 Recalled by Stryker...

The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Spectra-System/Legacy Guided Surgery Handle Kit Recalled by Implant Direct...

The Issue: The inside diameter of the 2.3mm small drill guide inserts have a smaller...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· Xintec Corp

Recalled Item: OptiLITE(TM) Products for Laser Surgery Recalled by Xintec Corp Due to It...

The Issue: It has been determined that the reprocessing instructions may not provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2017· International Medsurg Connection, Inc.

Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...

The Issue: Insufficient documentation to support product sterility claims.

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

Class II — Potential Health HazardOngoing