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. 2,469 recalls have been distributed to Indiana in the last 12 months.
Showing 41881–41900 of 53,528 recalls
Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...
The Issue: The recommended sterilization and drying parameters are not effective to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the monitor may fail and requires a power circle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...
The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: garden lites Veggie Chili & Cornbread Melt Recalled by classic cooking llc...
The Issue: Cumin contains undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: garden lites Southwestern Souffle Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden Lites Kale & Quinoa Souffle Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: classic cooking Kale and Quinoa Cake Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden Lites Veggie Bites Kale & Brown Rice Recalled by classic cooking llc...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend Recalled by...
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dark Chili Powder packaged in the following configurations: (1) a Recalled...
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Archer Farms Cumin Recalled by Brinkhoff & Monoson Inc Due to Undeclared Peanut
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely-depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Trifurcated Ext set Recalled by Churchill Medical Systems, Inc....
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Double Lumen Set with Bionector Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated Extension Set Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" High Pressure Set with Bionector Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.