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 28781–28800 of 55,602 recalls
Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...
The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision CRS Femoral LT SZ 5 Cemented Recalled by DePuy Orthopaedics,...
The Issue: There may be burrs on the extraction hole threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peaceful Mountain Recalled by Grato Holdings, Inc. Due to Multiple products...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formagere de la Brie brand Recalled by Cheezwhse/Com Due to Potential...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...
The Issue: Devices inappropriately displayed a low battery indicator determined to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...
The Issue: During a retrospective review of sterilization records, TriMed has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...
The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.