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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 25921–25940 of 29,947 recalls
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent (). The ZYM B reagent is Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NIH (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FB Reagent (). FB reagent is an additional test Recalled by BioMerieux SA...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: A customer reported that after upgrading to software version 3.5.5 from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia T and Symbia T2 computer tomography systems. These systems Recalled...
The Issue: There are confirmed reports of a component coming loose inside the CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...
The Issue: Geometric positioning error can occur after a rotational correction has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down....
The Issue: Remington Medical discovered an error on the FL-601-97 IFU; part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Oxylog 3000 plus ventilators Recalled by Draeger Medical Systems,...
The Issue: The potentiometers (knobs) for setting the ventilation parameters may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...
The Issue: Sterility of the product cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.