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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2058120600 of 48,219 recalls

DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: CVS Therapeutic Menthol Gel Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· Tris Pharma Inc.

Recalled Item: Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release...

The Issue: Superpotent Drug and Failed Stability Specifications: High...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Adult Glycerin Suppositories Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Wonder Freeze Pain Releiving Gel with ILEX Recalled by US Pharmaceuticals...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Lupin Pharmaceuticals Inc....

The Issue: Labeling: Missing label; Product complaints reported missing bottle label.

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Children Glycerin Suppositories Laxative for ages 2 to 5. Package Recalled...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: CRYO-273 Cold Pain Relieving Gel 128 FL. OZ. Distributed By: CRYO-273.com...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: Adult Glycerin Suppositories Recalled by US Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2019· US Pharmaceuticals Inc.

Recalled Item: CRYO-273 Cold Pain Relieving Gel Roll-On 3 FL. OZ. (89 Recalled by US...

The Issue: CGMP Deviations: Out of Specification results for either total microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 10, 2019· LNK International, Inc.

Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...

The Issue: Microbial contamination of non-sterile product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 10, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Lantis 8.3 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Lantis Commander Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Lantis system (pre-2003) Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Lantis 6.1 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...

The Issue: Potential of an open port in the quench venting system when using the...

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

Class II — Potential Health HazardOngoing