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.
4,312 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Feb 6, 2013
Extremity Medical, IO FiX System Accessory. Catalog Number 101-00010. This screw measuring device is an accessory to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Feb 6, 2013
45¿ Angle Driver / Z-H, Greatbatch Medical 10 000 Wahrie Drive, Clarance, NY 14031. Model #: P2661, P2662, T3635,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100. VITROS¿ Vapor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Kinnikinnick Pie Crust (frozen), Weight: 290 g/10 oz, Qty/Pkg: 2, Product packaged in a cardboard box with printed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.United Natural Foods, Inc. - Greenwood
FDA (openFDA food enforcement)
Reported Jan 30, 2013
Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit, Catalog # 24500, cartons of 20 kits, In-vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2013
Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Red Apple Slices 2.4 oz, Item #71746, 20 oz, Item # 71729 14 oz, Item # 71735. Item #71729 is sold under the brand name…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Unlimited Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 23, 2013
Brilliance 64 and Ingenuity CT Computed Tomography X-Ray Scanning Systems: Brilliance 64 - Model #728231; and Ingenuity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Sarns flexible arterial cannula, 6.7 mm (20Fr) OD with 3/8 in. connector, suture ring, 9.5 in (24 cm) long The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 16, 2013
ABX PENTRA ML, Software Versions: V8.0.x and Below; V.9.0.1 and V9.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments, Inc. dba Horiba Medical
FDA (openFDA device enforcement)
Reported Jan 16, 2013
Markets of Meijer 16oz Redskin Peanuts
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Meijer Distribution, Inc.
FDA (openFDA food enforcement)
Reported Jan 16, 2013
Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Multiexport Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 16, 2013
Immunoradiometric assay. Device is an immunoradiometric assay designed for the quantitative measurement of thyroid…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing circuit, 1.8m or 6 feet in length. Oxygen…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fisher & Paykel Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Analyzing system consists of a small and portable analyzer and plastic microcuvettes. The microcuvette contains…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.HemoCue AB
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Hemp Plus Granola. The product is packaged in a 25 lb. container. The UPC is 0 58449 88001 1. The product is labeled in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature'S Path Foods Inc.
FDA (openFDA food enforcement)
Reported Jan 2, 2013
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
FDA (openFDA device enforcement)
Reported Jan 2, 2013
GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal Patient Circuit Kit Disposable with Size…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 2, 2013
Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Curve catalog no.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Jan 2, 2013
Spence & Co New York-Style Nova Lox 4oz , refrigerated Spence & Co Smoked Salmon Trimmings, 2lb bulk…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spence & Co., Ltd.
FDA (openFDA food enforcement)
Reported Jan 2, 2013
Stryker Howmedica Osteonics; Stryker T2 Humerus System Teflon Tube, sterile; REF 1806-0073S The T2 Nailing System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Wound Therapy System. Major components of the AR1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arobella Medical, LLC
FDA (openFDA device enforcement)
Reported Dec 26, 2012
Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ebi, LLC
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.