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. 2,729 recalls have been distributed to Indiana in the last 12 months.
Showing 7861–7880 of 29,228 recalls
Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...
The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...
The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...
The Issue: Due to a non-sterile component (tape) being place within the sterile portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...
The Issue: Device does not meet regulatory requirements of stability while stationary,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...
The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FGFR RGQ RT-PCR Kit (RUO Recalled by Qiagen Sciences LLC Due to Increased...
The Issue: Increased occurrence rate of false positive results, lead to a false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen FGFR RGQ RT-PCR Kit (CE IVD Recalled by Qiagen Sciences LLC Due...
The Issue: Increased occurrence rate of false positive results, lead to a false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen FGFR RGQ RT-PCR kit (US IVD) Recalled by Qiagen Sciences LLC Due...
The Issue: Increased occurrence rate of false positive results, lead to a false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.