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.
4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported May 24, 2017
Moondance desserts gluten free Chocolate Chip Cookie Bar 12 oz (340g) UPC 36211 68096 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moondance Heavenly Desserts, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 24, 2017
Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Orthosoft, Inc. dba Zimmer CAS
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 24, 2017
WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported May 24, 2017
NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Almore International Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported May 17, 2017
NDI P7 Position Sensor, Stereotaxic Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported May 17, 2017
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported May 10, 2017
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 10, 2017
40/50 ct/kg (21/25 ct/lb) Farm Raised Head-On Shrimps, Keep Frozen, Must be fully cooked before serving. 1.02 kg, 2.24…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Global Marketing Enterprises, Inc.
FDA (openFDA food enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
Colby cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Meijer; Amish…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Deutsch Kase Haus, LLC
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Guggisberg Cheese Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 3, 2017
Maple Leaf Foods, Inc. Recalls Quiche Products Distributed Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maple Leaf Foods, Inc.
USDA FSIS
Reported May 3, 2017
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported Apr 26, 2017
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9
High riskUsing this product could cause serious injury, illness or death — stop using it now.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CP Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
GUGGISBERG NATURAL CHEESE COLBY INGREDIENTS: Pasteurized Milk, Cultures, Salt, Enzymes, Annatto Color 1 lb, 2 lb, 6 lb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dutch Valley Food Distributors
11 more products in this recall
FDA (openFDA food 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.