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 48,132 notices were distributed nationwide, so they reach Texas too — those are in the archive.

Medical devices

Reported May 24, 2017

GIZA Vertebral Body Replacement

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

Eden Spine Europe SA

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Food

Reported May 24, 2017

Kemps YO2 Frozen Yogurt Mudslide, One Pint, UPC 41483-04121

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

Kemps, LLC

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 24, 2017

enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

Navitrack¿ System - OS Knee Universal, Orthopedic Stereotaxic Instrument

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

Orthosoft, Inc. dba Zimmer CAS

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…

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

Almore International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Linear Straight Broach Handle (Rasp Handle) (Greatbatch Part # 510397; DJO Surgical Inc., # 803-03-159) and EZ Clean"…

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

Greatbatch Medical

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic…

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

Reser's Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 17, 2017

Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported May 17, 2017

Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…

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

Vertical Pharmaceuticals, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 17, 2017

Cobalt HV Bone Cement Cobalt MV Bone Cement Cobalt HV Bone Cement With Gentamicin

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported May 10, 2017

Kabob's Acquisition, Inc. Recalls Meat and Poultry Products Due to Possible Listeria Contamination

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

Kabobs Aquisition, LLC

USDA FSIS

Medical devices

Reported May 10, 2017

Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported May 10, 2017

H.E. B. brand Pomegranate Infused Cranberries COVERED IN Dark Chocolate, NET WT. 8 OZ. (227g), UPC CODE 041220985883

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

Nassau Candy

FDA (openFDA food enforcement)

Medical devices

Reported May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Food

Reported May 10, 2017

Precooked, chilled, Fresh Jumbo Lump Crabmeat, 1 lb, packaged in plastic container with plastic lid. King Crab and…

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

Seafarers Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 3, 2017

01.4mm x 457mm (18in) K-Wire, Threaded Blunt, Ref 9080B-18T, Qty: 1 per pack, Material: SS 316L, Full Temper, per ASTM…

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

Amendia, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX)…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Meat & poultry

Reported May 3, 2017

Blount Fine Foods, Corp. Recalls Beef Chile Colorado Frozen Meals Due to Misbranding and an Undeclared Allergen

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

Blount Fine Foods, Corp.

USDA FSIS

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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.