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. 997 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 39201–39220 of 55,602 recalls
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...
The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-piece Nebulizer with in-line connectors Recalled by Salter Labs Due to...
The Issue: Reports that the T-piece does not fit on the nebulizer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ottobock Modular Polycentric EBS Knee Joint 3R60 Recalled by Otto Bock...
The Issue: Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.