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 Feb 26, 2020
UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suja Life LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2020
OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
48 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
DaVinci Gourmet, Classic Caramel Flavored Sauce, 128 FL OZ (1 GAL), in plastic jugs
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kerry, Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Revanesse Versa, PN40081
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prollenium Medical Technologies Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sugar Foods Corporation
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Almark Foods, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Cocoon Convective Warming System, Product Code: CWS4000 (110V).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Care Essentials Pty., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Razzoo's Gumbo Base 10X4 LBS (1.8KG) Pouches Net Case Weight; 40 LBS STORE FROZEN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.National Food & Beverage, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Ranitidine Hydrochloride (powder), USP, Rx only, Spectrum Chemical Mfg Corp., a) 1 gram, b) 5 grams, c) 25 grams, d)100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Laboratory Products
FDA (openFDA drug 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.