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. 1,000 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,000 in last 12 months

Showing 17181–17200 of 48,219 recalls

Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N:...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 8Fr 50cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine HCL Gray/Yellow capsules Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Hydrochlorothiazide 50mg tablets Recalled by Calvin Scott & Company, Inc....

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine HCL White/Blue Speck Tabs 37.5 mg Recalled by Calvin Scott &...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine HCL White/Blue Speckled tablets Recalled by Calvin Scott &...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phendimetrazine Brown/Clear Capsules Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund