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. 2,768 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 17881–17900 of 29,947 recalls
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...
The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...
The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter...
The Issue: Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...
The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: North Star Imaging Inc. (NSI) Model X-7000 industrial cabinet x-ray Recalled...
The Issue: It was discovered a low-level radiation leak that was found on the NSI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: When a prior study is being replaced in the workflow step, in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis oneFloor-mounted system for uncompromised imaging Recalled by Siemens...
The Issue: The possibility exists for the monitor display of Artis one systems with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc....
The Issue: Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...
The Issue: Intermittent communication between the host system and the FlexCardio
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...
The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...
The Issue: Software update to correct several issues that include (1)Potential data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...
The Issue: Olympus has received complaints about fragments of adhesive which detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyOne Pro LAB VOS Respiratory Analysis System Pulmonary Function Testing...
The Issue: The CO/CO2 sensor cable harness may have lower electromagnetic shielding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.