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.

4,310 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Food

Reported Aug 17, 2016

Healthwise, Protein Chips, Barbecue Crunch, Net Weight 1.2 ounces (34 grams), Distributed by Nutritional Resources,…

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

Nutritional Resources Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2016

MX 16-slice whole body computed tomography X-ray system. Imaging diagnostic tool.

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

Philips Medical Systems (Cleveland) Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

Spirit Plus Bed, A-C Powered Hospital Bed

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

CHG Hospital Beds Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2016

Diced and sliced yellow onions. 2.5 lb & 5 lb clear plastic bags

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

Club Chef LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 10, 2016

Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

Synergy Cranial S7. The software application is sent in CD format with an IFU, wrapped in plastic with a label for…

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

Medtronic Navigation, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2016

ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 10, 2016

Lance Oyster Crackers, Dist. by Snyder's-Lance, Inc., Charlotte, NC 28277

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

S-L Snacks NC, LLC

FDA (openFDA food enforcement)

Food

Reported Aug 10, 2016

Kroger DELUXE ICE CREAM S'MORES 48 FL OZ (1.5 QT) 1.4 ML INGREDIENTS: ICE CREAM***GRAHAM COOKIES***CHOCOLATE…

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

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Aug 10, 2016

ROAST, NO SALT SUNFLOWER SEEDS sold under the following brands: Jungle Jim 16oz (453G) INGREDIENTS: SUNFLOWER SEEDS…

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

Windy Acres Candy & Nut, Outlet Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 10, 2016

Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates…

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

Zimmer Surgical Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 3, 2016

Sunflower Seeds, PLU# 65167; various weights; various sell by dates; Market District; Distributed by Giant Eagle,…

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

Giant Eagle, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 3, 2016

Integra External Fixation System Rocker Bottom Model # 12225400. For use in the treatment of bone conditions amenable…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300, Molift Air…

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

Moller Vital

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is a homogeneous enzyme immunoassay intended for use in…

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

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

SPHERICAL HEAD REFLECTION(R) 6.5 MM CANCELLOUS SCREW, REF 71332525, QTY: (1), STERILE R, smith&nephew Total hip…

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

BD Trucount Tubes: Catalog number: 340334 Hematology: BD Trucount tubes are used for determining absolute counts of…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

The sunflower kernels roasted and salted were packed in a 30 lbs. corrugated box with a poly liner with the following…

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

C.J. Dannemiller Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY TRAY…

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

Centurion Medical Products Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Frozen Organic Premium Sweet Baby Peas, Organic by Nature brand, net wt. 5 lb. The UPC is 8 46358 00063 3. Frozen IQF…

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

CRF Frozen Foods, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…

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

CSL Behring GmbH

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.