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 8781–8800 of 29,228 recalls
Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...
The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20545 Vitale Silver calcium Alginate Dressings 4x5 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20522 Vitale Silver calcium Alginate Dressings 2x2 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acufex Access Advanced Positioning Kit - indicated for use to Recalled by...
The Issue: Products were shipped to the Global Distribution Center instead of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXY-1 System Recalled by Abiomed, Inc. Due to The firm has received...
The Issue: The firm has received complaints of the OXY-1 System Console experiencing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches...
The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated Recalled by Collagen...
The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OER-Elite Endoscope Reprocessor-for use in cleaning and high-level...
The Issue: The detergent and alcohol tank tubing may have been incorrectly assembled in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EnPlace is a single use trans-vaginal pelvic floor repair Recalled by...
The Issue: Certain lots may not have been packaged wth the Channel Tube Limiter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VersaTips Recalled by Ortho-Clinical Diagnostics,...
The Issue: The lot has a shape deformity which may lead to a 16% reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERAKOS CELLEX Photopheresis Procedural Kit Recalled by Mallinckrodt...
The Issue: This recall was initiated to recover a Dunnage Case, which is a case of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.