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. 1,893 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,893 in last 12 months

Showing 4034140360 of 55,602 recalls

Medical DeviceOctober 1, 2015· Powers Medical Devices, LLC

Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...

The Issue: PAL unit has undergone significant technological changes since the previous...

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

Class II — Potential Health HazardOngoing
FoodOctober 1, 2015· Kontos Foods Inc.

Recalled Item: Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc....

The Issue: Kontos Falafel Mix contains undeclared wheat allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Strawberry Cream Cookies Recalled by Sobisk Foods LLC Due to...

The Issue: Strawberry Cream Cookies, imported from India, contain undeclared colors...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Lemon Cream Cookies Recalled by Sobisk Foods LLC Due to Undeclared Color

The Issue: Lemon Cream Cookies imported from India, contain undeclared color - FD & C...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 1, 2015· Sobisk Foods LLC

Recalled Item: Sobisk Orange Cream Cookies Recalled by Sobisk Foods LLC Due to Undeclared...

The Issue: Orange Cream Cookies, imported from India, contain undeclared colors...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 1, 2015· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: Reporting feature times out after inactivity for more than an hour sending...

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

Class II — Potential Health HazardOngoing
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2015· O-Two Medical Technologies, Inc.

Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...

The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...

The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Erroneous low results on a small number of reagent wells. There is the...

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

Class II — Potential Health HazardOngoing
FoodSeptember 30, 2015· Wyandot Inc

Recalled Item: Traditional Round Yellow Tortillas. Sold under the brand names of: Better...

The Issue: Firm was notified by a customer that the product contained an undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2015· Medtronic Inc.

Recalled Item: Medtronic Achieve Cables Recalled by Medtronic Inc. Due to 64 units of...

The Issue: 64 units of Achieve Electrical Cables were shipped with a potential...

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

Class II — Potential Health HazardOngoing
DrugSeptember 29, 2015· Hospira Inc.

Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 29, 2015· Fit Firm and Fabulous

Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund