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 May 3, 2023
JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT-PL 02 12-S, JLT-PL 02 14-S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spineart Sa
FDA (openFDA device enforcement)
Reported Apr 26, 2023
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Apr 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 26, 2023
Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Apr 26, 2023
AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 26, 2023
JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Apr 19, 2023
Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Agilent Technologies Inc./us
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP, Thermodilution Catheter, Exterior Diameter 8F…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2023
EMPOWR Porous Knee Patella Over Drill, REF: 802-05-104; EMPOWR Knee Patella Drill, REF: 802-05-108
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Hiland Fat Free Chocolate Milk Vitamin A&D Naturally Flavored Half Pint (236 mL) UPC 72060 00133 4 packaged in a paper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hiland Dairy Foods Company LLC
FDA (openFDA food enforcement)
Reported Apr 19, 2023
Flex-Neck Catheter External Repair Kit REF CE-1400 LOT CE-1400/A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Kagome Worcester Sauce 6/60 fl oz. Ingredients: Water, Sugar, Salt, Fermented Vinegar, Glucose, Tomato Extract, Caramel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mutual Trading Company Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2023
Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography (PET) and Computed Tomography (CT), Model uMI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Astor Chocolate Wafer Stick NWT WT. 11.64 OZ 330g UPC 72375102886
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Sysco Imperial Caesar Dressing NET CONTENTS 1 GAL (3.78 l) INGREDIENTS: Soybean Oil, Water, Distilled Vinegar, Parmesan…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Winland Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 12, 2023
FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand name: Shirakiku Distributed by: Wismettac…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wismettac Asian Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 5, 2023
Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Cirq Arm System 2.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Apr 5, 2023
COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
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.