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 Jun 18, 2025
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contamac Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Supreme Produce Celery & PB Snack Cup. Net Wt: 9oz (225g). Keep Refrigerated. UPC 8 50065-40308 3. GBC Food Services,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GBC Food Services, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microtek Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Mobility LLC
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NRC Nutrition Pty Ltd.
FDA (openFDA food enforcement)
Reported Jun 18, 2025
EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is a user controlled, stereotactic accessory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quantum Surgical Sas
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Best Taste Brand Salted Shrimp Paste Sauce; ING: Shrimp, sugar, salt; COUNTRY FAVOR, INC; PRODUCT OF VIETNAM; Net…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Country Favor Inc.
FDA (openFDA food enforcement)
Reported Jun 11, 2025
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GNC Holdings LLC
FDA (openFDA food enforcement)
Reported Jun 11, 2025
Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120 gummies/bottle); 12 bottles/case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Nordic Naturals, Inc.
FDA (openFDA food enforcement)
Reported Jun 4, 2025
Apo B Reagent, REF: OSR6143
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jun 4, 2025
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 4, 2025
VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 4, 2025
Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 4, 2025
Plus Initial Drill, Article Number: 103.170;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 4, 2025
Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultra Clean Systems, Inc.
FDA (openFDA device enforcement)
Reported May 28, 2025
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems, Inc.
FDA (openFDA device enforcement)
Reported May 28, 2025
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…
High riskUsing this product could cause serious injury, illness or death — stop using it now.C.R. Bard Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 21, 2025
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported May 21, 2025
H&C Farms Raw Premium Tomatoes, Naturally Grown from Seed Net WT 25 Lbs., 11.34 KG, packaged in cardboard box with lid,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hanshaw & Capling Farms, LLC
FDA (openFDA food enforcement)
Reported May 21, 2025
Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ray & Mascari,Inc.
FDA (openFDA food 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.