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. 2,560 recalls have been distributed to Indiana in the last 12 months.
Showing 25081–25100 of 53,528 recalls
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: Discoloration: Presence of dark discoloration or brown spots on the edges of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AF 550 x 5ML/HR 2ML 60LO CPNB Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF550x5ML/H 2ML 60LO 6" DUAL CATHS Recalled by Arrow International Inc Due...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...
The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-15LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...
The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB Recalled by Arrow International Inc...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H 6" DUAL CATHS Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Randox...
The Issue: Randox has previously issued a recall for Liquid Cardiac Control CQ5053 lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermacare HeatWraps Menstrual a) b) Product Recalled by Pfizer Inc. Due to...
The Issue: The firm received complaints of the wrap coming apart and leaking granular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H 6" CATH Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14ML/HR CPNB Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF w/AS 550 x 1-14 ml/hr Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 130 Deg 10x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 Deg 12x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.