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. 1,020 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,020 in last 12 months

Showing 15501–15520 of 48,219 recalls

Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
FoodMarch 8, 2021· New Generation Wellness Inc.

Recalled Item: Live Better vegan vitamin d-3 by CVS Health Recalled by New Generation...

The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...

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

Class III — Low RiskOngoing
Refund
FoodMarch 8, 2021· New Generation Wellness Inc.

Recalled Item: VEGAN VITAMIN D3 Recalled by New Generation Wellness Inc. Due to Vitamin D3...

The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2021· Akorn, Inc.

Recalled Item: Gabapentin Oral Solution Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - OUS Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 with Single Aspirate Autosampler (SMN 10316162) - OUS Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - OUS Recalled...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Boston Scientific Corporation

Recalled Item: MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter...

The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Boston Scientific Corporation

Recalled Item: MAMBA Microcatheter. Packaged with protective sleeve over catheter Recalled...

The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - OUS Recalled...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing