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.
4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Oct 20, 2021
Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 20, 2021
Green Field Farms Chocolate Milk 1/2 gallon glass jar, 6 units per case 53oz plastic bottle, 6 units per case 12oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Green Field Farms Co-op
FDA (openFDA food enforcement)
Reported Oct 20, 2021
Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 20, 2021
ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Ultrasound Transmission Clr 8.5 oz BTL 24/cs ECO 40JMC Gel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.National Distribution & Contracting Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 20, 2021
Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CardioQuip, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Oct 13, 2021
GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Djo, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Oct 13, 2021
Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Circulation, Inc.
27 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping 4oz, 6 containers per case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Central Kitchen Food Hub
FDA (openFDA food enforcement)
Reported Oct 6, 2021
Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper
FDA (openFDA food enforcement)
Reported Oct 6, 2021
Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.New Vision Pharmaceuticals LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 6, 2021
uMI 550 System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 6, 2021
Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Velvet Ice Cream Company
FDA (openFDA food enforcement)
Reported Sep 29, 2021
Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Sep 29, 2021
CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Sep 29, 2021
DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 29, 2021
cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Molecular Systems, Inc.
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.