Recalls distributed in Indiana
These notices name Indiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,305 stored notices name Indiana, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Sep 13, 2023
Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PBM Nutritionals, LLC
FDA (openFDA food enforcement)
Reported Sep 13, 2023
3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2023
GS70 Salus Surgical Table, Product Code 18-070-70
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2023
Link OptiStem Rasp Handle-Used with the OptiStem Rasp to prepare the femoral medullary canal for a knee prosthesis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
FDA (openFDA device enforcement)
Reported Aug 30, 2023
BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2023
The O-arm O2 Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
FDA (openFDA device enforcement)
Reported Aug 23, 2023
IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Aug 23, 2023
Newly Weds Foods R03810 LOEFFLER COMP PORK ROLL CURE X1 54lbs
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Newly Weds Foods, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 16, 2023
CD HORIZON Spinal System Solera Awl Tip Tap, REF NAV2006K
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Mom Donisi's Premium Dough on Parchment: packaged as 7in, 8in, 9in, 10in (thin), 10in (regular), 12 in (thin), 12in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cassanos Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 9, 2023
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Contour¿ next GEN Blood Glucose Monitoring System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascensia Diabetes Care US, Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722-3
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Jul 26, 2023
Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana, Strawberry, Mango, SKU #051191, packaged in pillow bags.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Scenic Fruit Company, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 26, 2023
Private Selection 48oz Classic Fruit Medley, frozen product, 8/48 oz bags per case. UPC 0 11110 82026 6. Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Townsend Farms Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 19, 2023
HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.