All recall categories

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.

Food

Reported Apr 20, 2016

Bumble Bee Chunk Light Tuna in Water, 48cans/case, 5oz, UPC 8660000020

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bumble Bee Foods LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 20, 2016

GE Healthcare, Aisys CS2 anesthesia..

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Medical Systems, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 20, 2016

#2473 CINCINNATI STYLE CHILI Savory Net Wt. 4 lbs (1.8kg) UPC 0 90939 12473 1 GOLD MEDAL PRODUCTS 10700 MEDALLION DRIVE…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gold Medal Products Co.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 20, 2016

Diana Automated Compounding System, Diana Onco Plus, Item No. ASN220 The Diana is an automated compounding device for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 20, 2016

Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 20, 2016

SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes (USA) Products LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 13, 2016

Country Life Natural Foods Labeled SHELLED PISTACHIOS RAW NET WT. 2lb (906 g) plastic bags item 030244 and Batch 1357…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Oak Haven, Inc. dba Country Life Natural Foods.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 13, 2016

A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 13, 2016

Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sweetwater Farms LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 13, 2016

Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Manufacturing B.V.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 7, 2016

Pilgrim’s Pride Corp. Retira Productos De Pollo Por Posible Contaminacin De Material Extrao

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pilgrim's Pride Corporation

USDA FSIS

Food

Reported Apr 6, 2016

MAGGI Chicken Flavor Bouillon 6Tab, 12Tab UPC Codes: 028000247959, 028000115678, 028000115678

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle USA

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 6, 2016

Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ossur H / F

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2016

The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…

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)

Medical devices

Reported Mar 30, 2016

Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2016

Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Spine, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Mar 23, 2016

Oxygen, Compressed USP (Gaseous, Medical Oxygen, Aluminum Cylinders), Packaged in a) M6-Tanks, b) D-Tanks, and c)…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Medical Park Homecare, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 23, 2016

Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2016

Bertolli Extra Virgin Olive Oil, 8.5 oz. and Carapelli Extra Virgin Olive Oil, 25.5 oz., packaged in glass bottles.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

DEOLEO USA, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2016

Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2016

Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Braga Organic Farms, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2016

Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mako Surgical Corporation

FDA (openFDA device enforcement)

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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.