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 Aug 28, 2019
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 28, 2019
SIGA Fresh Basil, 1 lb bag, 10 plastic bags (1 lb bag) per carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siga Logistics S de Rl de Cv
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BIMBO Bakeries USA Inc.
FDA (openFDA food enforcement)
Reported Aug 21, 2019
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Batter mixes labeled the following ways: 1) Batter, Item Number 30713419.49, Net Wt. 50 lb, Distributed by Kerry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry, Inc.
57 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 21, 2019
VAMPIRO V5001-minimally invasive poole suction sleeve that is an accessory instrument to ANY 5mm spot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Santanello Surgical LLC
FDA (openFDA device enforcement)
Reported Aug 21, 2019
Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
The Alinity ci-series System Control Modules which are configured with Alinity c Processing Modules. The Alinity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Aug 14, 2019
IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ideal Implant Incorporated
FDA (openFDA device enforcement)
Reported Aug 14, 2019
14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061423 Product Usage: An aid for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Ginger Spice, 1 oz (28.4 g), 2 oz, 4 oz, and 1-3 lb packages. An herbal tea, Taos, NM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milkweed & Monarch, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 14, 2019
Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories, Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage: The FERR Flex reagent cartridge is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wismettac Asian Foods, Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2019
Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Maximum Pelvic Trainer (MPT)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ralston Group
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Rusch EasyCath Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jul 31, 2019
ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
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.