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 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Mar 29, 2023
Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Russell Stover Candies Inc.
FDA (openFDA food enforcement)
Reported Mar 29, 2023
Haiyue Food Nutritional Preserved Vegetable
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Xiumin Lin
FDA (openFDA food enforcement)
Reported Mar 24, 2023
Elkhorn Valley Packing Recalls Boneless Beef Chuck Product Due to Possible E. coli O103 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elkhorn Valley Packing LLC
USDA FSIS
Reported Mar 22, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Fruit flavored ready-to-eat cereal packaged in 1.27 oz. (UPC 850017468214) and 8oz. ( UPC 850017468085) plastic stand…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Catalina Snacks
6 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Fusion Bioline Vascular Graft, Part number M00201503046B0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Mar 22, 2023
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mead Johnson & Company
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scientia Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2023
LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Given Imaging Ltd.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Preat Corp.
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Sensus Healthcare Inc, SRT-100 Vision IPX 0, HFUS Module IPX 1, with software version 1.9.2; Superficial X-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sensus Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alpenland International, Inc.
FDA (openFDA food enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706; EMPOWR VVC KNEE TIBIAL INSERT, SIZE 7, 22MM, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Mar 1, 2023
Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sovos Brands Intermediate, Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2023
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Access Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2023
Back To Nature Plant Based Snacks Fudge Mint Cookies Net Wt. 6.4 OZ. (181g) UPC code: 819898011025
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.B&G Foods North America, Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
SPiN Thoracic Navigation System Model: SYS-4000 (SYS-4000D)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
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.