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. 2,919 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 461–480 of 29,947 recalls
Recalled Item: Restore Clinician Programmer Application (CP App) Recalled by Medtronic...
The Issue: Software issue where a Device Reset message displayed on the app was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...
The Issue: Wire connected to the electrical box may shift out of its intended position,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...
The Issue: Wire connected to the electrical box may shift out of its intended position,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...
The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...
The Issue: When the Worstation of the BeneVision DMS has a specific hardware...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelerad InteleShare software Recalled by DICOM Grid, Inc. Due to Software...
The Issue: Software intended to aid in diagnosing conditions, planning treatments,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Da Vinci 5 ASSY Recalled by Intuitive Surgical, Inc. Due to An error event...
The Issue: An error event following the release of a software version for the surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...
The Issue: Customer complaints of Pressio monitor rebooting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix NorthStar OCT Navigation Surgical Technique Guide Recalled by...
The Issue: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.