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 9161–9180 of 29,228 recalls
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch Recalled by...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch Recalled by...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog # BEK4511 Recalled by Bard Peripheral Vascular Inc Due to Due to...
The Issue: Due to misbranded products shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog # BEK3411 Recalled by Bard Peripheral Vascular Inc Due to Due to...
The Issue: Due to misbranded products shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...
The Issue: Potential for a wire protrusion through the left heart vent catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.