All recall categories

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.

Medical devices

Reported Jul 27, 2022

Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

SX-One MicroKnife

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sonex Health LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2022

NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Synapse Biomedical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

AESCULAP TC COOELY MICRO NEEDLEHLDER SERR 200MM, product code MG524R. manual surgical instrument designed to grasp a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aesculap Implant Systems LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis US Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

HAMILTON-H900 Humidifier, Models: 950001, 950004

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Isopure Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2022

Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

J & M Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 20, 2022

MiniMed 620G Insulin Pump (O.U.S. version)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic device for the quantitative testing of samples of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Ventana HE 600 System, automated slide preparer, for use in laboratories.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2022

Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Waldemar Link GmbH & Co. KG (Mfg Site)

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2022

Slap Ya Mama Louisiana Food Products Slap Ya Mama Cajun Fish Fry packaged in a 5.5lb plastic container with plastic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Walker & Sons Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 20, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zeltiq Aesthetics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Omnera 400T Digital Radiographic System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arcoma AB

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien LLC

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 13, 2022

SoDelicious DairyFree Wondermilk Dairy Free Frozen Dessert Salted Caramel Sundae, 3 - 4 fl oz (12 fl oz) cones per…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Danone US LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 13, 2022

NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal, Model No. 08-2301-3

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Holdings, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 13, 2022

Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharmaceutical Industries,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Golden State Medical Supply Inc.

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jul 13, 2022

CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the enumeration of circulating tumor cells (CTC) of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Menarini Silicon Biosystems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

ABL800 Flex Analyzer Model Numbers 393-800 and 393-801

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2022

RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rayner Intraocular Lenses Ltd.

FDA (openFDA device enforcement)

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Other states

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.