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 13, 2022
SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corporation
FDA (openFDA device enforcement)
Reported Apr 13, 2022
First SIGN SARS-CoV-2 Antigen Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WHPM Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Gammex Non-Latex PI Green PI-KARE Skin-friendly PI Technology polyisoprene surgical gloves 7 1/2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
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 6, 2022
Elmer's Pecan Egg 1oz product wrapped in polypropylene wrapper and packaged into paper cartons packaged as singles, 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elmer Candy Corp.
FDA (openFDA food enforcement)
Reported Apr 6, 2022
Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Hanger-Bar 2P 45cm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Human Care USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Pneumonia (33 Targets) Control Panel, unassayed quality control material, containing: Positive Control 1 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RaySearch America Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
cobas LiatSystem, respiratory virus panel nucleic acid assay system, Material Number 07341920190
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz (113g). UPC 085239-182840 No Sulfites Added. No Artificial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suntree Snack Foods, LLC
FDA (openFDA food enforcement)
Reported Apr 6, 2022
EasyFuse Dynamic Compression System Instrument Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2022
BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 30, 2022
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2022
Shredded Cheese consisting of Monterey Jack, Queso Quesadilla, and Asadero cheeses, Net Wt 2lbs, packaged in plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schreiber Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 23, 2022
Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
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.