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 Apr 28, 2021
BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Trader Joe's Restaurant Style White Corn Tortilla Chips; Net Wt. 9 oz. (255g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snak King Corporation
FDA (openFDA food enforcement)
Reported Apr 28, 2021
Midline Catheter Dressing Change Kit with Statlock - Product Usage: Intended to provide ongoing vascular catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trinity Sterile, Inc.
FDA (openFDA device enforcement)
Reported Apr 28, 2021
KeVita Cucumber Rosemary (primary package), 15.2 oz., glass bottles, 6 packages per case, refrigerated storage
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropicana Products, Inc.
FDA (openFDA food enforcement)
Reported Apr 28, 2021
Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.USA Lanka Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 28, 2021
ELI 280 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn Inc. Mortara
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-union, mal-union, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
VIDAS¿ CMV IgM 30 Tests
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Apr 21, 2021
J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packages labeled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Apr 21, 2021
Disposable Sampling Tube, REF VSM01, Contents: Transport Media - 50, Nasal Swab - 50, Package Insert - 1, IVD, CE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Krishe Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Apr 14, 2021
MicroScan WalkAway-40 plus Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Amicus MNC Apheresis Kit - Double Needle - Product Usage: intended for use in the collection of blood components and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fenwal Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Drop Arm Versamode"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gf Health Products
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Panther Fusion Tube Tray, REF PRD-04000, PN: FA-15004, Cont. 18 Tube Trays - Product Usage: an ancillary consumable to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System, prosthesis, knee,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sharp Medical Products
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Ysio X.pree, Model Number: 11107464 - Product Usage: A Digital X-Ray System generate Xray images from the whole body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 14, 2021
Alaris Infusion Pump Module, Model 8100, serviced/repaired by Tenacor with an impacted bezel repair part
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tenacore LLC
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.