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. 1,978 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 26721–26740 of 55,602 recalls
Recalled Item: Solar 8000M Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 3000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: The system's IFU contains a list of generators that the have been deemed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...
The Issue: the Ball Cube II phantom calibration film was not manufactured within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The product was shipped after its expiry date due to a system error. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...
The Issue: The device has an offset in the design that results in a reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray BeneVision Distributed Monitoring System (DMS) Recalled by Mindray...
The Issue: The firm has identified performance anomalies with the device caused when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CedarLane Organic Salads Recalled by Cedarlane Natural Foods Inc/Frankly...
The Issue: Discovery that the product is labeled as gluten free but contains wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.