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 48,132 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.
Reported Sep 12, 2012
Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2012
16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bard Access Systems
FDA (openFDA device enforcement)
Reported Sep 5, 2012
V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. d.b.a. Mindray North America
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots 502058002 and 501318002 The Stratus(R) CS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory Packs (also commonly known as convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SRI Surgical
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Yellow onions Diced 3/8", packaged in 25-lb. plastic bags, 1 per case (item 19551); Diced 1/4", packaged in 5-lb. bags,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cool Creations, LLC
18 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 29, 2012
OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5, 8mm***STERILE***Match insert/spacer/tray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
FunFresh Foods World Berry Organic Cacao Nibs 6 oz, packaged in blue, brown, red, white, black and green packaging with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.FunFresh Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 15, 2012
djo surgical Screw 6.5 mm, Sz 25mm, low profile. Product is intended for the fixation of the acetabular shell or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Tartar Sauce sold under the following brand names: 1) Golden Corral Tartar Sauce, 1 gallon,refrigerated Product Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ken's Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2012
Sunrise Indian Corn Candy which is packaged in 16 oz clear plastic tubs/12 tubs per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mount Franklin Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2012
OXYGEN, COMPRESSED USP MEDICAL GAS in the following containers: E Cylinder 680L, D Cylinder 425L, and M6 Cylinder 165L,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oklahoma Respiratory Care Inc.
FDA (openFDA drug enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant (SJ780T-US) Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 8, 2012
The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Product is labeled in part: "***OPTETRAK***TIBIAL TRAY***TRAPEZOID CEMENTED***Ti Alloy*** SIZE 1F/1T, 2F/1T***FOR…
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 Aug 1, 2012
Hospira LifeShield Latex-Free 100 mL Burette Set, Convertible Pin, 77 inch with 2 Prepierced Injection Sites and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Leica M525 F50 Surgical Microscope; Article No. 10338422; Leica Microsystems (Schweiz) Ag, 201 Max Schmidheiny Strasse,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
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.