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. 2,878 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 5881–5900 of 29,947 recalls
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Assayed Chemistry Control Premium Plus Level 3 Recalled by Randox...
The Issue: there has been a transcription error in the Instructions for Use (IFU) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...
The Issue: It is possible the upper roller bracket in the Radixact System gantry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...
The Issue: Philips has identified three software issues with compliance concerns to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynCardia 50cc TAH-t Recalled by SynCardia Systems LLC Due to Artificial...
The Issue: Artificial hearts contain a epoxy resin that has not been reviewed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix¿ / Epidural anesthesia set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Product may be mislabeled with an incorrect lid stock label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.