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. 2,696 recalls have been distributed to Indiana in the last 12 months.
Showing 13461–13480 of 53,528 recalls
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...
The Issue: Software error may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...
The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Product: Product is contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Acetate Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...
The Issue: Presence of particulate matter: particulates composed of carbon and oxygen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per...
The Issue: Dietary supplement may contain potential metal shavings greater than or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...
The Issue: The product was distributed without FDA authorization or clearance for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....
The Issue: Software issue resulting in temporary loss of central monitoring functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...
The Issue: During the de-installation of an MR system magnet, if all rigging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m HBV AMP Kit (US and CE) Recalled by Abbott Molecular, Inc. Due to...
The Issue: There is a potential for misquantitation high results for negative samples.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...
The Issue: Sterility failure of the exterior of the syringe which may impact the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m HBV Application Specification File (US and CE) Recalled by Abbott...
The Issue: There is a potential for misquantitation high results of negative samples.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.