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. 1,896 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 39001–39020 of 55,602 recalls
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Bariatric Power Recliner Recalled by Hill-Rom, Inc. Due to The...
The Issue: The recliners were shipped without the foot rest ottoman linkage side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Recalled by Integrated Medical Systems Inc Due to If excessive...
The Issue: If excessive pressure is applied to the distal end of the endoscope, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeaterBaum Foot & Ankle Heating Pad Recalled by Ergoactives, Llc Due to...
The Issue: Products are marketed without a cleared 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...
The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits from Centurion that contain an In-Vision- Plus Needleless...
The Issue: Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...
The Issue: Failed Dissolution Specifications: Unexplained low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.