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 4136141380 of 55,602 recalls

Medical DeviceJuly 15, 2015· Medtronic Cardiovascular Surgery-the Heart Valve Division

Recalled Item: EnVeo R Loading System Recalled by Medtronic Cardiovascular Surgery-the...

The Issue: Medtronic is recalling the EnVeo R Loading Systems because of the presence...

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

Class I — Serious Health HazardOngoing
DrugJuly 14, 2015· KVK-Tech, Inc.

Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK-Tech, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 400 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: cobas b 123 Fluid Pack COOX 200 Product Recalled by Roche Diagnostics...

The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2015· Life and More LLC

Recalled Item: Akttive High Performance Fat Burner Gold dietary supplement capsules...

The Issue: Marketed Without An Approved NDA/ANDA: Dietary supplements contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 13, 2015· Perrigo Israel Pharmaceuticals

Recalled Item: Mometasone Furoate Ointment USP Recalled by Perrigo Israel Pharmaceuticals...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugJuly 13, 2015· Purdue Pharma L.P.

Recalled Item: Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Insulet Corporation

Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....

The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 13, 2015· Sedecal S.A.

Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....

The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2015· Draeger Medical, Inc.

Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...

The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2015· Etac Supply Center Ab

Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...

The Issue: The recalling firm has received reports of a malfunction of the Relax wall...

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

Class II — Potential Health HazardOngoing
FoodJuly 10, 2015· Maya Overseas Foods,Inc

Recalled Item: A Taste of the East maya brand Cashew Split Recalled by Maya Overseas...

The Issue: The cashews have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 10, 2015· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...

The Issue: Stryker Sustainability Solutions has received reports indicating that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...

The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Hardy Diagnostics

Recalled Item: HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Recalled by...

The Issue: Hardy Diagnostics is recalling HardyCHROm MRSA due to a report of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Cadence Inc.

Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...

The Issue: Graduation marks of the syringe are not centered with the numeric position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Cadence Inc.

Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...

The Issue: Graduation marks of the syringe are not centered with the numeric position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2015· Ivoclar Vivadent, Inc.

Recalled Item: IPS Empress Universal Glaze Spray 270 mL Recalled by Ivoclar Vivadent, Inc....

The Issue: Complaints were received of coarse particles in the glazed surface of IPS...

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

Class II — Potential Health HazardOngoing
FoodJuly 8, 2015· Fresh Unlimited Inc

Recalled Item: Caesar Salad Recalled by Fresh Unlimited Inc Due to The firm failed to...

The Issue: The firm failed to declare the allergen eggs on their labels.

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

Class I — Serious Health HazardOngoing
Refund