Recalls distributed in Oklahoma
These notices name Oklahoma 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.
2,997 stored notices name Oklahoma, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.
Reported May 16, 2018
Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
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
ReNew Dolphin Nose Disposable Dissector Tip, Catalog Number: 3312, UDI: 00811099011989 The ReNew single patient use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microline Surgical, Inc.
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
Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziegenfelder Company, Inc.
1 more product in this recall
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 4, 2018
Eddy Packing Co., Inc. Recalls Smoked Sausage Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eddy Packing Co., Inc.
USDA FSIS
Reported May 2, 2018
Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU 6500009 Used to achieve epithelial graft in the oral cavity.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ace Surgical Supply Co., Inc.
FDA (openFDA device enforcement)
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
Cali Green Malay Kratom all packages, all quantities
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutrizone LLC
9 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
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)
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 11, 2018
Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Harvest, Inc.
FDA (openFDA food enforcement)
Reported Apr 11, 2018
Alpha Air 6 ENT Microscope Microscope examination of the human ear, nose, and throat.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seiler Instr. & Mfg. Co. Inc.
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
Product Name Lot Number or ID Whiskey & Cola Type Flavored Seasoning 660373
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Griffith Foods
7 more products in this recall
FDA (openFDA food 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
Taylor Farms 3/8" Diced Yellow Onion 4/5# bags - 20 lb, corrugated paper carton; 20 lb. box for food service…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms California Foodservice, 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.