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. 2,919 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 561–580 of 55,602 recalls
Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...
The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148 Recalled by Philips...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T. Product Code (REF): (1) 781342 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...
The Issue: Complaints received that Vanta A71200 CP App does not function as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...
The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 Recalled by CareFusion...
The Issue: Due a software issue that may result in equipment not receiving timely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lost and Found Energy Recalled by Fazt & Loud LLC Due to Recall is due to a...
The Issue: Recall is due to a misprint on the label that incorrectly identifies the...
Recommended Action: Do not consume. Return to store for a refund or discard.