Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,086 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,086 in last 12 months

Showing 17801–17820 of 55,602 recalls

Medical DeviceMarch 8, 2021· BIOTRONIK Inc

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

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 ILIVIA NEO 7 VR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

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 Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...

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 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 INTICA NEO 7 VR-T DX DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

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 Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

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 Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

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 ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

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 INTICA NEO 7 HF-T DF-1 IS-1 ProMRI Recalled by BIOTRONIK Inc Due...

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 Ilestro 7 VR-T DX Recalled by BIOTRONIK Inc Due to There is a...

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 ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

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: 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
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 5, 2021· HU PRODUCTS

Recalled Item: Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g)...

The Issue: Product may contain undeclared almonds.

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

Class II — Potential Health HazardOngoing
Refund
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 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 with Single Aspirate Autosampler (SMN 10316162) - 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 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 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
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