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 Mar 15, 2017
CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Metrex Research, LLC.
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Parker Medical
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Roth Net Polyp Retrieval
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bell Stone Toffee
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
McKesson Radiology 12.2 - Picture Archive Communication System (PACS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Imaging
FDA (openFDA device enforcement)
Reported Mar 8, 2017
SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MED-EL Elektromedizinische Gereate, GmbH
FDA (openFDA device enforcement)
Reported Mar 8, 2017
DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
EliA Sample Diluent, Article number, 83-1023-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Deep River Sour Cream & Onion Krinkle Kettle Chips 2 oz bag UPC 8 50668 00049 8 & 5 oz bag UPC 8 50668 00099 3
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shearers Foods, LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 8, 2017
PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
123 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Theravits 100, container sizes: 30, 60, 90, 180, Product Code: 0783-30, 0786-60, 0789-90, 0788-180; The Supreme One,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Organic Corp.
FDA (openFDA food enforcement)
Reported Mar 2, 2017
Ohio Farms Packing Co. Ltd. Recalls Veal Products Due To Possible E. Coli O103 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ohio Farms Packing Co. Ltd.
USDA FSIS
Reported Mar 1, 2017
AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Applied Medical Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet U.K., Ltd.
23 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Flake Snack Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 1, 2017
Levothyroxine Sodium 135 mcg/Liothyronine 15 mcg SR capsules, 90 count bottles, Rx only, Moore's Pharmacy Compounding,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moore's Compounding Pharmacy
FDA (openFDA drug 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.