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. 968 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 45921–45940 of 55,602 recalls
Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...
The Issue: Technical Support Bulletin issued in February 2013 did not mention...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rejuvenator Chamber manufactured by Baro-Therapies Recalled by...
The Issue: The firm is distributing the Rejuvenator device without an approved 510(k).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Respiratory Modules E-sCO Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUBICIN (daptomycin for injection) 500 mg Recalled by Cubist...
The Issue: Presence of Particulate Matter: Foreign particulate matter (tiny black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5%...
The Issue: Presence of Particulate Matter: particulate matter was found during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...
The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-HCV Reagent Pack for in vitro...
The Issue: VITROS Immunodiagnostic Products Anti-HCV kit lot 9090 has been observed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.