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. 2,342 recalls have been distributed to Wyoming in the last 12 months.
Showing 35381–35400 of 48,219 recalls
Recalled Item: Major loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Up&Up loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Pharmacy Recalled by Ohm Laboratories, Inc. Due to Superpotent Drug: Out...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Pharmacy loratadine orally disintegrating tablets USP Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equaline Original Prescription Strength Recalled by Ohm Laboratories, Inc....
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Premier Value Loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Access Thyroglobulin Assay Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter, Inc. is recalling Access Thyroglobulin reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics...
The Issue: When both ports (Serial and Ethernet) are configured to transmit data, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for z-statistic related to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doubletree Cookie Dough Recalled by Christie Cookie Co Inc Due to Reports of...
The Issue: Reports of clear and green plastic pieces in cookies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...
The Issue: Low red blood cell control recoveries and low results for red blood cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.