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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 27641–27660 of 53,528 recalls
Recalled Item: LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....
The Issue: Presence of Particulate matter. Recall due to presence of unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park...
The Issue: Presence of Particulate matter. Recall due to presence of unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr....
The Issue: Presence of Particulate matter. Recall due to presence of unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...
The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...
The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...
The Issue: The DC power to the IFOSS collision detector control panel at your facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...
The Issue: Unusually high number of total images/unassigned events may require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 801 immunoassay analyzer Recalled by Roche Diagnostics Corporation...
The Issue: The syringe plunger on the device may be mounted in a tilted position, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar...
The Issue: There is a potential dry blast irregularity on the locking collar screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WipeEssentials Wet Wipes (benzalkonium chloride 0.13%) Recalled by Diamond...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACURE Recalled by Diamond Wipes International, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...
The Issue: The connector of the power supply was capable of fitting other components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...
The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.