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.

4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,124 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Jun 12, 2013

E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology

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

Kreg Medical Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jun 12, 2013

Lorazepam, 0.5 mg tablets, 100 count, RX only, Distributed by Major Pharmaceuticals, Livonia, MI. NDC 0904-6007-60

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Legacy Pharmaceutical Packaging LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 12, 2013

Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…

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

Maytex Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…

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

Angiodynamics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2013

Meijer Diced Pears in Fruit Juice 8oz cup

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Meijer Distribution, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2013

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

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

Nephron Pharmaceuticals Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…

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

Orthovita, Inc., dba Stryker Orthobiologics.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2013

Talenti Roman Raspberry Sorbetto, 16fl oz, Crafted by Talenti, Marietta, GA 30062

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

Talenti Gelato

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Rostorelle L, Polypropylene Mesh, Catalog number 501440, Manufacturer Coloplast A/S 3050 Denmark.

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Food

Reported May 29, 2013

Krinos TAHINI ground sesame seeds, 1) Net. Wt. 1 lb (454g) in glass jars with gold lids packed 12 jars per case - UPC…

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

Krinos Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2013

Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…

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

Linvatec Corp. dba ConMed Linvatec

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated…

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

Progressive Medical Inc.

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Stryker Orthopaedics Triathlon Femoral Distal Augment- Left; 1 single unit per package Howmedica Osteonics Corp. 325…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…

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

American Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported May 22, 2013

Grippo's Potato Chips, 1oz, 1 1/8oz , 1¿oz, 3.5oz, 8oz, 12oz bags & 1.5lb boxes, INGREDIENTS: SELECTED POTATOES,…

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

Grippo Potato Chip Co., Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

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

Heartware Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes work like a ceiling light while…

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

Insight Instruments, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. The Vistakon (etafilcon A) Soft (hydrophilic)…

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

Johnson & Johnson Vision Care, Inc.

1 more product in this recall

FDA (openFDA device 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.