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 May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MHC Medical Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Munk Pack Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Soozie s Doozies Sugar Cinnamon Snickerdoodle Cookie Dough, 16 ounce, plastic pouch, 6 pouches per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.National Foodworks Services
FDA (openFDA food enforcement)
Reported May 16, 2018
NeoBase Succinylacetone Assay Solution, Product Number: 3042-0020; Affected UDI Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported May 16, 2018
ACUSON SC2000 Ultrasound System. The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 16, 2018
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Smoked Salmon Spread 5 lb. bulk units; Simply Superior Smoked Salmon Spread 5 oz units; and Morey s Smoked Salmon…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Superior Foods Company
FDA (openFDA food enforcement)
Reported May 9, 2018
StoneBreaker Pneumatic Lithotripter, Catalog number: SBL-KIT1; GPN: G52604 UDI:(01)00827002526044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 9, 2018
Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IntroMedic Co., Ltd.
FDA (openFDA device enforcement)
Reported May 9, 2018
Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mccall Farms Inc.
FDA (openFDA food enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported May 9, 2018
Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperVision Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sofradim Production
FDA (openFDA device enforcement)
Reported May 2, 2018Updated Oct 23, 2026
JBS USA, Inc. Recalls Ground Beef Products Due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Swift Beef Company
USDA FSIS
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Human Fetal Hemoglobin (HBF-1) FITC Conjugate
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Midwest Northern Nut Roasted Salted Natural Almonds. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midwest Northern Inc.
65 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2018
SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smucker Natural Foods, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The J.M. Smucker Company, Inc.
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Indiana recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.