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. 2,792 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 15461–15480 of 29,947 recalls
Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PremierPro Aluminum Adjustable Walker Recalled by SVS LLC Due to This recall...
The Issue: This recall is due to a mandated order from the FDA for stock recovery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P28 Recalled by Paragon 28, Inc. Due to Mislabeling
The Issue: It has been determined that the wedge implant kit is permanently mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...
The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Locking Drill Guide Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Hex Driver 1.2 Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...
The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...
The Issue: There is a possibility that the liquid suction pump on some AIA-2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Thermal Chamber Motor Cable located in the following models:...
The Issue: Thermal chamber motors have electrical cables with single insulation rather...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.