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 Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Angiographic Guidewire Component: Model Number: 107042, 107044, 107447, 110003, 110004, The angiographic guidewire…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
28 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Garlic Alfredo Sauce. Product code 20607981. Keep Frozen. Net Wt. 30 lb. (13.61KG) Distributed By: Kerry Inc., Beloit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry Global Technology Innovation Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 9, 2021
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hi Tech Pharmaceuticals
FDA (openFDA food enforcement)
Reported Jun 9, 2021
***Chicken Street Taco Kit with Trays, item # 13454.38080, Refrigerated product, 2/4.985 lbs. kits in each case.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported Jun 2, 2021
Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jun 2, 2021
NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare Procera LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 2, 2021
BiPAP V30 Auto, US market: Continuous ventilator, non-life-supporting. Material Number: 1111178
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Respironics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 2, 2021
PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jun 2, 2021
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 26, 2021
REF 7617400, Groshong NXT ClearVue Catheter, intermediate kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741045094 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported May 26, 2021
ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hi Tech Pharmaceuticals
13 more products in this recall
FDA (openFDA food enforcement)
Reported May 26, 2021
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Public Goods
FDA (openFDA food enforcement)
Reported May 26, 2021
Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage: intended to aid in the diagnosis of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 26, 2021
GORE VIBIL Biliary Endoprosthesis: stents, drains and dilators for the biliary ducts. Catalogue numbers: VH1008040,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W.L. Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported May 26, 2021
Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WillowWood Global LLC
FDA (openFDA device enforcement)
Reported May 19, 2021
Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atos Medical AB
FDA (openFDA device enforcement)
Reported May 19, 2021
PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
Panera Lobster Bisque, 16 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blount Fine Foods Corporation
FDA (openFDA food enforcement)
Reported May 19, 2021
REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
25 more products in this recall
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.