All recall categories

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.

Medical devices

Reported Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ready Pac Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 19, 2020

Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sugar Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Niti-S Esophageal Stent, REF ES1806F, ES1808F, ES1810F, ES1815F, ES2006B, ES2010B, ES1612B, ES1615B, ES1810B, ES1812B,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Taewoong Medical Co., Ltd.

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Datascope Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Fresh Grab Ham & Swiss on Pretzel Sub Bun, 6 oz., UPC: 612510001028

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lipari Foods Operating Company, LLC.

31 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 12, 2020

ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles ( NDC 43063-844-14); b) 30-count bottles (NDC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PD-Rx Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 12, 2020

PediaLift Access Device, Device Identifier: B751PDLFT0

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PediaLift LLC

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Fresh Location Protein Snack Tray 6.44oz, UPC: 8-5511000804-6

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The H.T. Hackney Co. LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Sienna Chocolate Turtle Brownie (frozen); 108 OZ (6.75 LB) Uncut, 4 trays per case; UPC: 93901541857 SSC:10093901541854

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Dianne's Fine Desserts

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Drugs

Reported Feb 5, 2020

Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

McGuff Compounding Pharmacy Services, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Feb 5, 2020

AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Drugs

Reported Jan 29, 2020

Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 150 mg, a) 30 count bottles (NDC: 68788-7388-3), b) 60 count…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Preferred Pharmaceuticals, Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Meat & poultry

Reported Jan 24, 2020

Amity Packing Company Inc. Retira Productos De Carne Molida Cruda Debido A Una Posible Contaminación Con Materia Extraña

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amity Packing Co. Inc.

USDA FSIS

Medical devices

Reported Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2020

Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gourmet International Ltd.

FDA (openFDA food enforcement)

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Other states

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.