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. 1,008 recalls have been distributed to Indiana in the last 12 months.
Showing 37321–37340 of 53,528 recalls
Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...
The Issue: Drager became aware of situations where the error message "Poti unplugged"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...
The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...
The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...
The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.