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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 26761–26780 of 29,947 recalls
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...
The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...
The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....
The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...
The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...
The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...
The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.