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. 2,747 recalls have been distributed to Indiana in the last 12 months.
Showing 4721–4740 of 53,528 recalls
Recalled Item: MySyrup Sugar Free Almond Syrup. Product is packaged in the Recalled by My...
The Issue: Acidified product is recalled due to lack production record.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MyChai Chai Tea Concentrate KALI Recalled by My Chai Inc Due to Acidified...
The Issue: Acidified Chai Tea products are recalled because pH was found above 4.1 and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MySyrup Sugar Free Raspberry Syrup. Product is packaged in the Recalled by...
The Issue: Acidified product is recalled due to lack production record.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MyChai Chai Tea Concentrate Double. Product is packaged in the Recalled by...
The Issue: Acidified Chai Tea product is recalled due to lack production record.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MySyrup Sugar Free Coconut Syrup. Product is packaged in the Recalled by My...
The Issue: Acidified product is recalled due to lack production record.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MySyrup Sugar Free Hazelnut Syrup. Product is packaged in the Recalled by My...
The Issue: Acidified product is recalled due to lack production record.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL Recalled by...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug- An out of specification ( OOS ) result observed in assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...
The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...
The Issue: It was discovered during device performance testing that the CCD imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...
The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. Versions 13.0 Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Just Right 5000 Recalled by Elevate Oral Care Due to LABELING: LABEL MIX-UP.
The Issue: LABELING: LABEL MIX-UP.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Miami J Select Collar Recalled by Ossur H / F Due to Pressure sensitive...
The Issue: Pressure sensitive adhesive hooks attached to the sides of the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.