Recalls distributed in Texas
These notices name Texas 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.
6,720 stored notices name Texas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,124 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Mar 21, 2018
Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 21, 2018
NaturaLyte¿ Liquid Acid Concentrate 2.0 mEq/L, Model # 08-2251-0 3.43 liter bottle This concentrate is formulated to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Cakes, LLC
FDA (openFDA food enforcement)
Reported Mar 21, 2018
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Buttermilk Pancake and Waffle Mix, Item number: 6170B25, packaged in 25 lbs. bulk kraft bag. The label is read in…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bob's Red Mill Natural Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 14, 2018
241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cypress Medical Products LLC
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Vardenafil HCl, USP (trihydrate), 500 GM Part # 330-05, Rx only, For Manufacturing, Repackaging and Processing for Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kalchem International, Inc.
FDA (openFDA drug enforcement)
Reported Mar 14, 2018
O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Springside Cheese Corp.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 14, 2018
Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters, Ref D134301,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitalab Co. Inc.
FDA (openFDA food enforcement)
Reported Mar 14, 2018
Dark Chocolate Covered Almonds 9 oz clam shell & 25 lb box Ingredients: Dark Chocolate (Sugar, chocolate Liquor, Cocoa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Alternatives LLC
FDA (openFDA food enforcement)
Reported Mar 14, 2018
Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2018
Heartland Catfish Company Recalls Siluriformes Fish Products Due to Possible Adulteration
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heartland Catfish Company, LLC
USDA FSIS
Reported Mar 7, 2018
Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Mar 7, 2018
AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avid Medical, Inc.
22 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Sterile EXACTAMED Oral Dispenser, Clear, Individually Packaged, 5 mL, Product Code H93876105
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Better-Bladder cardiopulmonary bypass blood reservoir; Models: BB14 (individual, sterile, pouched) and BB14NS (sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Circulatory Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
1 more product 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.