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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 16261–16280 of 53,528 recalls
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...
The Issue: Claim for stability after reconstitution from lyophilized to liquid form...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WishBone Medical Plate and Screw System - Screw Recalled by Wishbone...
The Issue: Nonconformities were discovered to the engineering specifications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...
The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...
The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garden Cut Coleslaw W/ Carrot Organic Recalled by Indianapolis Fruit...
The Issue: Foreign material in product (plastic)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim Recalled...
The Issue: Ingredient tested positive for milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...
The Issue: undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrostatic Filter Angled Recalled by Covidien, LP Due to The company was...
The Issue: The company was notified by their supplier of sterilization services for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CB10W65R1 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY10D90R2 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic BB7D76R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8R62R13 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HY8M63R4 Recalled by Medtronic Perfusion Systems Due to Specific...
The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.