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 Apr 25, 2018
Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 18, 2018
AUTO REF/KERATOMETER ARK-1s
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Apr 18, 2018
Normed Charcot Osteotome Chisel (Various sizes)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
FDA (openFDA device enforcement)
Reported Apr 14, 2018Updated Oct 23, 2026
Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Food Manufacturing Company
USDA FSIS
Reported Apr 11, 2018
Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Apr 11, 2018
Elecsys BRAHMS PCT Immunoassay for the in vitro quantitative determination of PCT (procalcitonin) in human serum and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Apr 11, 2018
King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The King Arthur Flour Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 7, 2018
J.T.M. Provisions Company Retira De Productos De Carne De Res Debido A Una Posible Contaminacin Con Materia Externa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J.T.M. Provisions Company
USDA FSIS
Reported Apr 4, 2018
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
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 Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A7AP, UDI: 04560141940031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Konica Minolta Medical Imaging USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Apr 4, 2018
The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SIE AG, Surgical Instrument Engineering
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Southgate Hot Dog Chili Sauce 15 oz cans UPC 0 71846 95242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vietti Acquisitions, LLC
FDA (openFDA food enforcement)
Reported Apr 4, 2018
Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
19 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2018
Good Foods Group, LLC Retira Productos De Pollo Listos Para Consumir Debido A Un Error De Rotulacin Y Un Alrgeno No…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Good Foods Group, LLC
USDA FSIS
Reported Mar 31, 2018
PFP Enterprises LLC Retira Productos De Carne De Res Cruda Producidos Sin El Beneficio De La Inspeccin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Patterson TMP Operating, LLC
USDA FSIS
Reported Mar 28, 2018
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Malecot and the Stenting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 28, 2018
ClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Insights, LLC
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.