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. 1,784 recalls have been distributed to Indiana in the last 12 months.
Showing 43241–43260 of 53,528 recalls
Recalled Item: Caviar Medley/Garden Vegetable 12/36 oz Product number 10610 Recalled by...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 16 oz. Jalapeno Jack Queso Dip Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Crate & Barrel 11.5 oz. Monterey Jack Queso Dip Recalled by Riba Foods Inc...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 11.5 oz. Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Black Bean Nacho Recalled by Riba Foods Inc Due to Undeclared...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...
The Issue: Defective container: A customer complaint revealed the presence of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...
The Issue: An increase in complaint trending for a loss of audible sound associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...
The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...
The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...
The Issue: Unintended treatment termination could result from a keypad malfunction in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.