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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 2201–2220 of 53,528 recalls
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Granules...
The Issue: Failed Dissolution Specifications: Product failed to meet dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Blood Products Administration Set Dual-Inlet Recalled by Fresenius Kabi...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PILLAR SA Ti Recalled by Orthofix U.S. LLC Due to A 37 mm implant width...
The Issue: A 37 mm implant width intervertebral body fusion device has a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preat Recalled by Preat Corp Due to Due to manufacturing error, digital...
The Issue: Due to manufacturing error, digital analog rotational feature is 180 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Recalled by Thoratec...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number:...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...
The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical...
The Issue: The DFPM yoke assembly ("yoke assembly") may detach from the spring arm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR System Software. Model Number: 444829. Recalled by Becton Dickinson &...
The Issue: Potential for functionality issue that supports the Over labeling feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor Bedside SpO2 Patient Monitoring System: Recalled by...
The Issue: Bedside SpO2 Patient Monitoring System alarms not heard/recognized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Recalled by...
The Issue: Clear coat seal on the lid of the single serve cups did not get applied...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg Recalled by Lupin...
The Issue: Product Mix Up: This product is being recalled because of a complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent Drug: Assay below the approved specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent Drug: Assay below the approved specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent Drug: Assay below the approved specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.