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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 48,100 notices were distributed nationwide, so they reach Oklahoma too — those are in the archive.

Medical devices

Reported Jan 8, 2025

3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…

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

3M Unitek Corporation

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2025

--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…

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

Grimmway Enterprises, Inc. dba Grimmway Farms

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 8, 2025

Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. Each kit contains 6 Pitas, Gyro Meat,…

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

Reser's Fine Foods, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 8, 2025

Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.

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

Sprouts Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…

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

Abbott Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…

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

Becton, Dickinson and Company, BD Bio Sciences

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…

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

Straight Smile, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Duravent Silicone Ventilation Tube. Model Number: 240075.

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Dec 20, 2024

Ralph's Packing Company Recalls Ready-To-Eat Pork and Beef Bologna Products Due to Misbranding and an Undeclared…

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

Ralph's Packing Company

USDA FSIS

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

Microscissor Tip (Disposable); Microline Catalog #: 3122.

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

Microline Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

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

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)

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

Cartiva, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2024

AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA…

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

Dyma Brands

20 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

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

Curio Spice Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL

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

Shimadzu Corp. Analytical & Measuring Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

a) Alcon Custom-Pak CONSTELLATION 25G PLUS CHRISTIANA CARE HLTH SERV, # 15340-11, containing TUBING, SALEM SUMP, 14 FR;…

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2024

Chicken Alfredo Kit

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

Joseph Seviroli, LLC

FDA (openFDA food 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.