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. 2,364 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,364 in last 12 months

Showing 3192131940 of 48,219 recalls

Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...

The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...

The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN...

The Issue: Eight (8) issues were identified which may affect the results generated by...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2016· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -...

The Issue: Subpotent Drug: Out of Specification assay values on stability for the...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2016· Stratus Pharmaceuticals Inc

Recalled Item: Remeven Cream Recalled by Stratus Pharmaceuticals Inc Due to...

The Issue: Crystallization; Complaints that cream appears to have crystallized

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

Class III — Low RiskOngoing
Refund
DrugMay 25, 2016· Sandoz Inc

Recalled Item: Lisinopril Tablets USP Recalled by Sandoz Inc Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 25, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...

The Issue: Software displayed incorrect prior reports in the viewport area, only when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...

The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...

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

Class II — Potential Health HazardOngoing
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: TASTE BUDS SEASONED FLOUR Recalled by Magic Seasoning Blends, LLC Due to...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: OUTBACK STEAKHOUSE OSI Mama's Batter Recalled by Magic Seasoning Blends, LLC...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: WOW 101 TENDER BATTER Recalled by Magic Seasoning Blends, LLC Due to There...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: OUTBACK STEAKHOUSE COMPLETE BREADING MIX Recalled by Magic Seasoning Blends,...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: OUTBACK STEAKHOUSE CRAWFISH/CHICKEN/CALAMARI BREADER Recalled by Magic...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2016· Magic Seasoning Blends, LLC

Recalled Item: ONION BREADER Recalled by Magic Seasoning Blends, LLC Due to There is a...

The Issue: There is a potential presence of peanut protein in certain lots of milled...

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

Class II — Potential Health HazardOngoing
Refund