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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 28561–28580 of 53,528 recalls
Recalled Item: A&W All American Food Papa Sauce Recalled by Ventura Foods, LLC Due to...
The Issue: A plastic foreign object was inadvertently introduced into the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: plastic cup with foil seal: House Recipe Bleu Cheese Dressing & Dip Recalled...
The Issue: A plastic foreign object was inadvertently introduced into the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...
The Issue: Defective Container: products showed leakage (bubbles, foaming) of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...
The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...
The Issue: It was discovered that in certain situations, including partial sessions and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Choceur Dark Chocolate Bars Recalled by Aldi Inc Due to Undeclared Treenut
The Issue: ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HERB-OX Beef Flavor Granulated Bouillon Recalled by Creative Contract...
The Issue: Creative Contract Packaging LLC is voluntarily recalling two code dates of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pantoprazole Sodium for Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viokace (pancrelipase) tablets Recalled by ALLERGAN Due to Subpotent Drug:...
The Issue: Subpotent Drug: One lot of Viokace is being recalled since product stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...
The Issue: There is a risk of circuit board breakage within the main housing of the AC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.