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. 2,383 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,383 in last 12 months

Showing 2284122860 of 48,219 recalls

DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 2, 2018· Baxter Healthcare Corporation

Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Stephanix

Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...

The Issue: The firm has detected a potential risk using the command. After releasing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Virtual Imaging, Inc.

Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...

The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...

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

Class II — Potential Health HazardOngoing
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 1, 2018· LivaNova USA Inc.

Recalled Item: SORIN Heater-Cooler System 3T 120V~/60Hz Description of product: Recalled by...

The Issue: The firm has become aware that due to a chemical reaction, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· R & D Systems, Inc.

Recalled Item: Quantikine¿ IVD¿ ELISA Recalled by R & D Systems, Inc. Due to The Human sTfR...

The Issue: The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was...

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

Class III — Low RiskOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· Boston Scientific Corporation

Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...

The Issue: Experienced accelerated battery depletion and a shortened replacement...

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

Class II — Potential Health HazardOngoing