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. 1,053 recalls have been distributed to Indiana in the last 12 months.
Showing 23221–23240 of 53,528 recalls
Recalled Item: Rim Plate Recalled by I.T.S. GmbH Due to The titanium implant has the wrong...
The Issue: The titanium implant has the wrong article number laser marked on it.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...
The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anastrozole Tablets Recalled by American Health Packaging Due to GMP...
The Issue: GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: First Step Draco Pad Recalled by Madison Polymeric Engineering Due to This...
The Issue: This product has been contaminated with Stenotrophomonas lactiubi.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent...
The Issue: This product has been contaminated with Stenotrophomonas lactiubi.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasal Alar SpO2 Sensor Recalled by Xhale Assurance, Inc. Due to These...
The Issue: These Instructions for Use has missing instructions related to the checking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...
The Issue: User may suffer an electric shock when coming in contact with the exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...
The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...
The Issue: Potential issue related to the operation of the safety latch within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...
The Issue: The deparaffinization solution contains a contaminant, which leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Beast Recalled by Stiff Boy LLC Due to Undeclared Sildenafil
The Issue: Marketed without an Approved NDA/ANDA: The Beast contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senna (sennosides 8.8 mg) Syrup Recalled by Geritrex, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles Recalled by...
The Issue: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 1 mg Recalled by Zydus Pharmaceuticals...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 0.25 mg Recalled by Zydus...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Zydus...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Anastrozole Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to CGMP...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MethylPREDNISolone Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: CGMP Deviations: Cross Contamination with other products due to CGMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.