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. 2,663 recalls have been distributed to Indiana in the last 12 months.
Showing 14821–14840 of 53,528 recalls
Recalled Item: Teg Creme Cake Bag 50#. Material #4107664 Recalled by Puratos Corporation...
The Issue: Product may be contaminated with foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sliced Pickled Beets Recalled by Seneca Foods Corporation Due to Lack of...
The Issue: Lack of acidulant.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Easy Satin Creme Cake Bag 50#. Material #4107811 Recalled by Puratos...
The Issue: Product may be contaminated with foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NSA Creme Cake Bag 50#. Material #4107591 Recalled by Puratos Corporation...
The Issue: Product may be contaminated with foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TK019 2017 Choc Cup Powder Blend Bag 50#. Item number 4005543 Recalled by...
The Issue: Product may be contaminated with foreign material (metal)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...
The Issue: The Instructions for Use have been updated to include: (1) Clarification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...
The Issue: Due to consoles not in compliance with the latest electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...
The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...
The Issue: It was noticed in production on 28.10.2021, that the final testing database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...
The Issue: Labelling: Incorrect Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml) Recalled...
The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.