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 48,122 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Sep 26, 2018
Freedom EV0-2 with any version of EVOware and EVOware Sample Tracking Add-On V1.0 or higher
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2018
La Planta De Procesamiento Junior's Smokehouse Retira Productos De Cesina De Res Debido A La Posible Contaminacin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Junior's Smokehouse Processing Plant
USDA FSIS
Reported Sep 19, 2018
Beaver Accu-Temp High Temperature Cautery, 2 inch Shaft with Fine Tip, Model Number 8445000 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec
FDA (openFDA device enforcement)
Reported Sep 19, 2018
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2018
Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. 6 OZ paper bag Dewey's BAKERY WINSTON-SALEM, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dewey's Bakery, Inc. dba Salem Baking Company
FDA (openFDA food enforcement)
Reported Sep 19, 2018
da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 19, 2018
AnastoClip GC Closure System, REF# 4007-08 a closure system designed to penetrate the outer layers of tissue during the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2018
ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIUM, Model THS-LX-C…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics Inc., dba Ev3 Neurovascular
FDA (openFDA device enforcement)
Reported Sep 19, 2018
Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SPS Sterilization, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 19, 2018
Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 280 mm, Item Number: 814309280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
128 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alden Optical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
VidiStar(TM) PACS & DICOM Viewer Software system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Healthcare Americas Corp. Informatics Division
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inspire Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and data processing.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Israel Ltd.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. box .
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mojave Foods Corp.
FDA (openFDA food enforcement)
Reported Sep 12, 2018
AutoDELFIA Neonatal immunoreactive trypsin(ogen) (IRT) kit, intended for the quantitative determination of human…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Virtus Pharmaceuticals Llc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 12, 2018
Outer Package Label: Tapered Screw-Vent Implant System, 4.1mm X 10mm, 3.5mm, REF:TSVM4B10, Sterile:R, Rx Only; Inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Dental Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Sep 5, 2018
FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare 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.