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. 991 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 42821–42840 of 55,602 recalls
Recalled Item: Lipo Pack Recalled by Stradis Healthcare, LLC. Due to Convenience kits being...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shoulder Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovenous Kit Recalled by Stradis Healthcare, LLC. Due to Convenience kits...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasc Custom Kit - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skin and Vein Pack - contains Devon Light Glove Used during surgery Recalled...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Pack and General Surgery Pack - contains Devon Light Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head & Neck Pack - contains Devon Light Glove Used during surgery Recalled...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blepharoplasty Pack - contains Devon Light Glove Used during surgery...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Transfer Set w/MicroClave T-Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 108" (274 cm) Transfer Set w/Check Valve Recalled by ICU Medical, Inc. Due...
The Issue: ICU Medical is recalling MicroClave T-Connectors because they have potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chlordiazepoxide HCl/Clidinium Bromide capsules Recalled by Valeant...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Librax (5 mg chlordiazepoxide HCl and 2.5 mg clidinium bromide) capsules...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: High out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.