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.
Reported Sep 2, 2020
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
The following products received from the UNFI Distribution Center Champaign, IL on 7/12/2020: Ditch Farms Eggs brand:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
HAVEN'S KITCHEN***GOLDEN TURMERIC TAHINI***NET WT 5oz (142g)***Ingredients: Water, Tahini, Extra Virgin Olive Oil,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Haven'S Kitchen
FDA (openFDA food enforcement)
Reported Aug 26, 2020
HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3 oz***KEEP FROZEN***10004302***PRODUCT OF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.High Liner Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Gluten-Free Organic Mesa Sunrise Cereal USA, Nature's Path brand. Shop Order # 127895. Product is Ready to eat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures Path Foods USA, Inc.
FDA (openFDA food enforcement)
Reported Aug 26, 2020
Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Garden Cut Organic Coleslaw w/ Carrots, retail unit packaged in 1lb clam-shell, 4 retail units per wholesale case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Indianapolis Fruit Company, Inc.
FDA (openFDA food enforcement)
Reported Aug 19, 2020
Marketside Peanut Butter Brownie, Net Wt. 19 oz, Distributed by Walmart Inc. Bentonville, AR
Moderate riskThis product could cause temporary or reversible health problems — stop using it.James Skinner Baking Co.
FDA (openFDA food enforcement)
Reported Aug 19, 2020
AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Linet Americas
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Tibial knee prosthesis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellements LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 12, 2020
BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are single use devices intended to clean the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Remisol Advance running Software Version 1.12 The Normand Info Remisol Advance Data Manager collects and manages data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Khaotan Rice Cracker, Net Wt. 150g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siam Trading Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2020
SUTUREFIX ULTRA Suture, Product number 72203855
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sutter Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Giant Eagle Dried Island Fruit Mix , Net Wt. 10 oz. , 6 units per case. Packaging is a gusseted plastic resealable bag.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Giant Eagle
FDA (openFDA food enforcement)
Reported Aug 5, 2020
Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
Computed Tomography X-ray System; Model uCT 760; Rx; UDI: (01) GTIN: 06971576831043 - Product Usage: intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
2 more products 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.