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

Medical devices

Reported Jun 12, 2024

Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor

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

Verathon, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

BD Pyxis MedStation ES, REF: 323, Medication Cabinet

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

CareFusion 303, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, Software Version Number 8.1.100.

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

Philips Medical Systems Nederland B.v.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2024

Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 Trevo XP ProVue…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 29, 2024

Sammy's Milk GOAT MILK TODDLER FORMULA, 25.68 oz (78g) pouch

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

Graceleigh, Inc. dba Sammy's Milk

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported May 29, 2024

chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g

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

Kairo's Group, Inc. dba Chuao Chocolatier

FDA (openFDA food enforcement)

Drugs

Reported May 29, 2024

Duloxetine Delayed-Release Cap USP 30mg, 30-count bottle, Rx only, Preferred Pharmaceutcals, Inc., NDC 68788-9301-03

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

Preferred Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 22, 2024

Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US

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

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2024

HeartSine samaritan PAD (Public Access Defibrillator), Type: SAM 350P, SAM 360P, SAM 450P

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported May 22, 2024

Jalapenos packed in 6lb 10oz cans. 6 cans per case

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

M-C McLANE INTERNATIONAL

FDA (openFDA food enforcement)

Food

Reported May 22, 2024

Sensible Portions brand Garden Veggie Straws Sea Salt. 1 oz bag UPC:2951530057 Packaged in a 30 CT Variety Pack that…

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

The Hain Celestial Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2024

TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm,…

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

TriMed Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2024

GE Healthcare Innova IGS 5, computed tomography x-ray system

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

GE Medical Systems, SCS

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2024

5000 Compact Series Ultrasound Systems, Product/REF: 5500 CV/795141, 5500 P/795143, 5500 W/795144, 5500 G/795145, and…

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

Philips Ultrasound, Inc.

FDA (openFDA device enforcement)

Food

Reported May 15, 2024

Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Medical devices

Reported May 8, 2024

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

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

Allergan Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Medtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100, REF: PMAC71RIC

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

Covidien

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2024

Thoratec HeartMate 3, LVAS Implant Kit, REF:106524US, Sterile EO, RxOnly

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

Thoratec Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom…

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Food

Reported May 1, 2024

12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case

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

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

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

Quidel Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

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.