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. 2,667 recalls have been distributed to Indiana in the last 12 months.
Showing 14321–14340 of 53,528 recalls
Recalled Item: "Juicing Greens" (salad product) packed in 11oz. packages Recalled by Fresh...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Organic Herb Mix" (salad product) packed in 5oz. packages Recalled by Fresh...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Green Leaf Shreds" (salad product) packed in 4.5oz. packages Recalled by...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: "Chopped Avocado Ranch" (salad product) packed in 12.3oz. Recalled by Fresh...
The Issue: potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...
The Issue: Due to 16 complaints related to drivers not engaging in implants. According...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...
The Issue: The firm has received six (6) complaint reports from customers indicating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Digital Angiography System Bransist safire Generator Model D150GC-40...
The Issue: Due to the inadequate adjusting criteria in installation, the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Angiography System Shimadzu Trinias Generator Model: D150GC-40...
The Issue: Due to the inadequate adjusting criteria in installation, the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...
The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clobetasol Propionate Ointment USP Recalled by Taro Pharmaceuticals U.S.A.,...
The Issue: Microbial Contamination of Non-Sterile Products: presence of R. Pickettii...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 20545 Vitale Silver calcium Alginate Dressings 4x5 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20522 Vitale Silver calcium Alginate Dressings 2x2 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acufex Access Advanced Positioning Kit - indicated for use to Recalled by...
The Issue: Products were shipped to the Global Distribution Center instead of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXY-1 System Recalled by Abiomed, Inc. Due to The firm has received...
The Issue: The firm has received complaints of the OXY-1 System Console experiencing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches...
The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated Recalled by Collagen...
The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.