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 Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2017
Vinh Hoan USA, Inc. Recalls Siluriformes Fish Products Due To Failure To Comply With FSIS Import Requirements
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vinh Hoan USA, Inc.
USDA FSIS
Reported Jun 21, 2017
Chocolate chip cookie dough larabars, 10 count , UPC 100-21908-49031 incorrectly packaged in peanut butter cookie…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Simple truth Dry Roasted Macadamia Nuts SEA SALT 12 oz bag UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Jun 20, 2017
Channel Fish Processing Co., Inc. Recalls Siluriformes Fish Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Channel Fish Processing Co., Inc.
USDA FSIS
Reported Jun 14, 2017
California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola…
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Sun Dry Foods
FDA (openFDA food enforcement)
Reported Jun 14, 2017
DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 7, 2017
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Kite Hill Mushroom and Ricotta Ravioli; frozen Ravioli made with almond milk ricotta: 9 oz. package. UPC 856624004173…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyrical Foods Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2017
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2017
Creation Gardens Inc. Recalls Ground Beef and Beef Primal Cut Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Creation Gardens
USDA FSIS
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to be used to acquire,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phoenix Food, LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2017
Armour Eckrich Meats, LLC Recalls Ready-To-Eat Sausage Products Due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Armour Eckrich Meats, LLC
USDA FSIS
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
GIZA Vertebral Body Replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eden Spine Europe SA
FDA (openFDA device enforcement)
Reported May 24, 2017
White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk; 20pk/Cs. Intended for packing and absorption externally or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
1 more product in this recall
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.