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. 2,604 recalls have been distributed to Indiana in the last 12 months.
Showing 18021–18040 of 53,528 recalls
Recalled Item: Seasonal Fruit Tray 40oz packaged in a clear plastic container Recalled by...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Apple 14oz Recalled by Country Fresh Inc. Due to Potential Listeria...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cantaloupe Chunks 16oz Recalled by Country Fresh Inc. Due to Potential...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Seasonal Blend 10oz Recalled by Country Fresh Inc. Due to Potential Listeria...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mango Spears 16 oz Recalled by Country Fresh Inc. Due to Potential Listeria...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pineapple Recalled by Country Fresh Inc. Due to Potential Listeria Contamination
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...
The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...
The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...
The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...
The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...
The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...
The Issue: Due to a change in handle material and process, probe handle may crack.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy¿ AspireSR¿ Generator Recalled by LivaNova USA Inc Due to Due to...
The Issue: Due to an extra digit being inadvertently added to the serial number of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKIPPY Super Chunk Peanut Butter 16.3oz packaged in Recalled by Hormel Foods...
The Issue: Aflatoxin level slightly above actionable limit
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...
The Issue: Failed Impurities/Degradation - Out-of-specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.