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 Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
AVID Medical QA Pack AV10654-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avid Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chobani
FDA (openFDA food enforcement)
Reported Feb 14, 2018
SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2018
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J F C International Inc.
FDA (openFDA food enforcement)
Reported Feb 14, 2018
SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventura Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2018
DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dollar General Corporation, Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Manicaretti Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Jan 31, 2018
Nestle HOT POCKETS¿ FOUR CHEESE PIZZA SNACK BITES in clear plastic bags.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle USA
FDA (openFDA food enforcement)
Reported Jan 31, 2018
Syngo Imaging version V31 (model # 10014063) is a Picture Archiving and Communication System (PACS) intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2018
ACCOLADE SR Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2018
Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 17, 2018
UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp. dba Ambu, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Sundream 12 V tanning bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSun International, LLC
FDA (openFDA device enforcement)
Reported Jan 3, 2018
Sterile Elastic Esmark Bandage, 3" x 9", individually packaged in a Tyvek plastic form fill seal pouch and placed into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Oklahoma recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.