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 19, 2024
US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of water to be used for hemodialysis Vivonic Part Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2024
MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Medical Systems Israel, Functional Imaging
FDA (openFDA device enforcement)
Reported Jun 19, 2024
Grande Lactose SKU 30600. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose Contains Milk. Grande Custom…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grande Cheese Company
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 19, 2024
Scallop Pot Seas 703161, 860 kg. SAP Code: 30589206. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kerry, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 19, 2024
VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs Calibrator Pack contains 3 X labelled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARROW INTERNATIONAL Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Germantown Stabilizer 1772-II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.Danisco USA Inc.
35 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2024
GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ADULT, 1 TB BAYONET,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Nussloch GmbH
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Costco Chocolate Chunk Frozen Cookie Dough, Net Wt. 33lb (14.97kg), 1.6 oz dough pucks Member's Mark Chocolate Chunk,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rise Baking Company dba South Coast Baking
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2024
Cream Cheese Spread. Keep Refrigerated, packaged under the following brands: 1. Dunkin, Net Wt 8 oz. (226g), UPC 0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schreiber Foods Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 12, 2024
The Synchro Neuro Guidewires are a steerable guidewire family with a shapeable tip. The outside diameter of the Synchro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2024
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2024
WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop Software with Instruction Manual and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WAVi Co.
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 5, 2024
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2024
Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2024
Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Channel Medsystems, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2024
SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2024
Sammy's Milk GOAT MILK TODDLER FORMULA, 25.68 oz (78g) pouch
High riskUsing this product could cause serious injury, illness or death — stop using it now.Graceleigh, Inc. dba Sammy's Milk
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 29, 2024
chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Kairo's Group, Inc. dba Chuao Chocolatier
FDA (openFDA food enforcement)
Reported May 29, 2024
IMMULITE 2000 Anti-TG Ab Catalog # L2KTG2 (200 Tests), SMN 10381659, System, Test, Thyroid Autoantibody.
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)
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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.