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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3708137100 of 48,219 recalls

FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Deluxe Mixed Nuts with Sea Salt: Aurora Recalled by Aurora Products, Inc....

The Issue: Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2015· Aurora Products, Inc.

Recalled Item: Roasted Mixed Nuts No Salt: Gourmet Garage Recalled by Aurora Products, Inc....

The Issue: Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 20, 2015· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2015· CooperSurgical, Inc.

Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...

The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2015· Biosense Webster, Inc.

Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...

The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2015· Mylan Institutional LLC

Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2015· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2015· Biomet, Inc.

Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...

The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2015· Akorn, Inc.

Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....

The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 17, 2015· Trader Joes Company

Recalled Item: Trader Joe's Nuts Raw California Walnut Pieces NET WT. 16oz. Recalled by...

The Issue: The firm is recalling Raw Walnuts because the products have the potential to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 17, 2015· Kraft Foods Group Inc.

Recalled Item: Kraft Macaroni & Cheese Boxed Dinner Original Flavor Recalled by Kraft Foods...

The Issue: This voluntary recall has been initiated because Kraft Macaroni & Cheese...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems....

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems...

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray...

The Issue: A head holder released for use with other CT systems but not yet qualified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2015· Biocare Medical, LLC

Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...

The Issue: A drop in staining intensity over time has been observed. These lots may not...

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

Class II — Potential Health HazardOngoing