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 5601–5620 of 29,947 recalls
Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...
The Issue: A high recovery of Iron assay has been observed at some customer sites....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Iron Reagent Recalled by Sentinel CH SpA Due to A high recovery of...
The Issue: A high recovery of Iron assay has been observed at some customer sites....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...
The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope Recalled by Boston Scientific...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The...
The Issue: Due to a software anomaly which potentially could result in the surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6 Recalled by Smith &...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS ARTICULAR INSERT Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPOINT 500 Blood Gas System Recalled by Siemens Healthcare Diagnostics...
The Issue: There are potential drug interferences from Perhexiline Maleate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPOINT 500e Blood Gas System Recalled by Siemens Healthcare Diagnostics...
The Issue: There are potential drug interferences from Perhexiline Maleate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV Recalled by B. Braun Medical, Inc....
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.