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. 1,035 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 29481–29500 of 55,602 recalls
Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Oncology) - Model no. 728243 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM...
The Issue: Data has shown that degradation of a raw material used in Phantom Fiber may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...
The Issue: Device may display a battery missing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Fetal Hemoglobin (HBF-1) FITC Conjugate Recalled by Life Technologies...
The Issue: Three lots of Human Fetal Hemoglobin FITC Conjugate are displaying high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...
The Issue: The manufacturer received complaints indicating that the device's central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weis Weis Markets Recalled by WEIS MARKETS Due to Undeclared Egg
The Issue: Label does not list sub-ingredients for mayo and sour cream The product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Recalled by eBars...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MAN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.8 OZ (51g) Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.