Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,741 recalls have been distributed to Indiana in the last 12 months.
Showing 5521–5540 of 29,228 recalls
Recalled Item: EVO+VISIAN Implantable Collamer Lens Recalled by Staar Surgical Company Due...
The Issue: Their is a potential that intraocular implant devices may not meet...
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: 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: DJO EMPOWR Knee Punch Handle Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee punch handle tip is breaking during surgery due to the lack of heat...
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: 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: 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: 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 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: 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: 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.