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 48,132 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Sep 27, 2017
Laxmi Rusks, 10.58 OZ (300 gram) bags; UPC Code: 7 23246 26482 0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.House
FDA (openFDA food enforcement)
Reported Sep 27, 2017
K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The K-ASSAY(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kelejete LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Honest Kids Juice Slushy Blueberry Punch, 3.5-oz. pouch, UPC 0065762211116.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coca-Cola Company
FDA (openFDA food enforcement)
Reported Sep 20, 2017
BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Sep 20, 2017
New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bestherbs Coffee LLC
FDA (openFDA drug enforcement)
Reported Sep 20, 2017
eMAG System, Ref 418591 It is an In Vitro Diagnostic Medical device intended for the automated isolation (purification…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Richmond Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion. Product Usage: Multifunction electrode for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Leonhard Lang Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Doctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hydrochloride) Syrup,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mid Valley Pharmaceutical
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Southeastern Mills Custom Seasoning Solutions
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 13, 2017
JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanmore Implants Worldwide Ltd.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Gazab Green Raisins, 7 oz. 14 oz. packages, 20/25 packs/carton
High riskUsing this product could cause serious injury, illness or death — stop using it now.United Trading Inc.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ameditech Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gold Medal Products Co.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
POLYURETHANE ENFit(R) AMERITUS NG FEEDING TUBE, REF Numbers: a) ENF-50P-40 b) ENF-50P-50 c) ENF-50P-80 d) ENF-60P-40 e)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kentec Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mary's Gone Crackers, Inc.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
CIVCO Arm Support, REF 106015, distributed as: (a) Rigid Arm Support, Standard, Set Red (PN: 106015) (b) Rigid Adj. Arm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med Tec Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2017
mcompass 2-channel Balloon Catheters The mcompass Biofeedback Anorectal Manometry System is for use on patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medspira, 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.