The Recall Desk

State

Texas product recalls

72,919 recalls have nationwide distribution and so reach Texas. 12,389 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,389
Critical
1,705
Severe
2,407
Most recent
2026-09-09

Of the 12,389 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.

These figures cover only the 12,389 recalls whose distribution notice names Texas specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2251–2275 of 85308

  • ModerateFDA (Devices)·Z-1956-2026·2026-05-06

    Philips Ingenia 1.5T MRI System Stiffness Value Calculation Error Recall

    Philips Ingenia 1.5T MRI systems with MR Elastography may display incorrect stiffness values and voxel size settings due to image reconstruction parameter combinations. The error affects 54 units distributed worldwide.

    Product
    Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model Number (REF): 781396. 4. Model Number (REF): 782115. 510(k) Numbers: K163116, K173079, K183063, K193215, K213583, K223458, K251397, K251808
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2026·2026-05-06

    Philips Ingenia 3.0T MRI System with Elastography Software Recall

    Philips Ingenia 3.0T MRI systems with MR Elastography software may display incorrect stiffness values and voxel size settings when specific image reconstruction parameters are used, potentially affecting diagnostic accuracy.

    Product
    Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model Number (REF): 782103. 510(k) Numbers: K163116, K173079, K183063, K193215, K213516, K213583, K223458, K251397, K251808
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0504-2026·2026-05-06

    Fentanyl Citrate Injectable Solution Recalled for cGMP Deviations

    Wells Pharma of Houston is voluntarily recalling 2,940 IV bags of fentanyl citrate injectable solution due to cGMP (current good manufacturing practice) deviations. The product was distributed nationwide.

    Product
    fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag, wells pharma of Houston, NDC 73702-202-03.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1952-2026·2026-05-06

    Philips Achieva 1.5T MRI System MRE Protocol Parameter Error Recall

    Philips Achieva 1.5T MRI systems with MR Elastography may display incorrect stiffness values and voxel size settings when certain image reconstruction parameters are used together, potentially affecting diagnostic accuracy.

    Product
    Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0679-2026·2026-05-06

    Negita shrimp crackers contain undeclared FD&C Yellow 6

    Negita Cracker Shrimp 2.8 oz is being recalled because the product contains undeclared FD&C Yellow 6. 142 units are affected.

    Product
    Negita Cracker- Shrimp 2.8oz
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-1964-2026·2026-05-06

    Philips MR 7700 MR Elastography device stiffness value error recall

    Philips is recalling certain MR 7700 devices with MR Elastography due to potential stiffness value errors when specific image reconstruction parameters are used, which may cause voxel size settings to display incorrectly.

    Product
    Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2003-2026·2026-05-06

    Philips Bridge Prep Kit catheter may experience resistance during advancement

    Merit Medical Systems is recalling the Philips Bridge Prep Kit (REF K12-09098C) because the catheter may experience resistance when advanced over the guidewire, potentially affecting proper device function.

    Product
    Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0685-2026·2026-05-06

    Calypso Tropic Tango Lemonade contains undeclared Yellow No. 5

    Calypso Tropic Tango Lemonade is being recalled because it contains undeclared Yellow No. 5. The action covers 299,779 cases distributed nationwide and to four other markets.

    Product
    Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King Juice Company, Inc., Milwaukee, Wisconsin 53221.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0526-2026·2026-05-06

    Alendronate Sodium Oral Solution Recalled for Out-of-Specification Assay Results

    Hikma Pharmaceuticals USA Inc. is recalling Alendronate Sodium Oral Solution 70 mg/75 mL due to out-of-specification assay results found in a limited number of bottles. The affected lot (AC2040A) was distributed nationwide.

    Product
    ALENDRONATE SODIUM — ALENDRONATE SODIUM (ALENDRONATE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1950-2026·2026-05-06

    HiResolution Bionic Ear Battery Pak Fails Safety Door Compliance

    Advanced Bionics is recalling HiResolution Bionic Ear System M Zn-Air Battery Paks because the non-tamperproof battery door does not require a tool to open, violating safety standards. The issue affects 45,173 units distributed worldwide.

    Product
    Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110; CI-5501-120; CI-5501-130; CI-5501-140; CI-5501-150; CI-5501-190; CI-5501-240; CI-5501-250; CI-5501-260; CI-5501-270; CI-5501-280 Software Version: Not Applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0500-2026·2026-05-06

    iVIZIA Dry Eye Lubricant Drops Recalled for Sterility Assurance

    Thea Pharma, Inc. is recalling iVIZIA Dry Eye (Povidone 0.5%) lubricant eye drops nationwide due to the FDA's discovery of manufacturing process deviations that affect the product's sterility assurance.

    Product
    IVIZIA DRY EYE — IVIZIA DRY EYE (POVIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0507-2026·2026-05-06

    Ketamine Hydrochloride Injectable Solution Recalled for cGMP Deviations

    Wells Pharma of Houston LLC is recalling 4,975 syringes of Ketamine Hydrochloride Injectable Solution (50 mg/mL) distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations.

    Product
    Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1965-2026·2026-05-06

    Philips SmartPath to dStream MR Elastography System Reconstruction Error

    Philips is recalling certain SmartPath to dStream 1.5T MR Elastography systems due to potential stiffness value errors when specific image reconstruction parameters are used, which may cause incorrect voxel size settings in the default MRE scan protocol.

    Product
    Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0494-2026·2026-05-06

    Levocarnitine Injection USP Missing Label Recall

    American Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.

    Product
    LEVOCARNITINE — LEVOCARNITINE (LEVOCARNITINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1998-2026·2026-05-06

    Heraeus PALAMIX duo dental mixing system batches worldwide recall

    Heraeus Medical is recalling PALAMIX duo dental mixing units (Material Number 66057897) because the mixing rod may come loose from its lock during use in units older than 1.5 years. The shelf life is being reduced from 3 years to 1.5 years.

    Product
    Heraeus, PALAMIX duo. Material Number: 66057897.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1997-2026·2026-05-06

    Heraeus PALAMIX uno Dental Material Mixing Rod Loose Risk Recall

    Heraeus Medical is recalling PALAMIX uno dental material because the mixing rod may come loose during mixing in units older than 1.5 years. The shelf life has been reduced from 3 years to 1.5 years.

    Product
    Heraeus, PALAMIX uno. Material Number: 66057893.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0509-2026·2026-05-06

    CVS Lidocaine Wound Gel recalled for failed pH specifications

    CVS Lidocaine Wound Gel is being recalled because it failed pH specifications. The affected product is distributed nationwide.

    Product
    Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V285000·2026-05-05

    Winnebago Recalls 2026-2027 Solis RVs Due to LP Hose Routing Defect

    Winnebago is recalling 2026-2027 Solis recreational vehicles because the liquid propane hose may be routed over the exhaust heat shield, posing a fire risk.

    Product
    WINNEBAGO — WINNEBAGO SOLIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V284000·2026-05-05

    Utilimaster Velocity Recalled for Incorrect Cargo Capacity Label

    Shyft Group is recalling 2025 Utilimaster Velocity vehicles because the cargo carrying capacity label may list an incorrect load value, potentially leading to overloading.

    Product
    UTILIMASTER — UTILIMASTER VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V283000·2026-05-04

    Tesla rearview camera image may be delayed when reverse is selected

    Tesla is recalling certain vehicles running software version 2026.8.6 because the rearview camera image may be delayed when the vehicle is placed in reverse, breaching FMVSS 111.

    Product
    TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V282000·2026-05-04

    2026 Toyota 4Runner Vehicles Recalled Due to Incorrect Load Capacity Label

    Gulf States Toyota, Inc. is recalling certain 2026 Toyota 4Runner vehicles because the load carrying capacity label is incorrect. This error may lead to improper vehicle loading and increase the risk of a crash.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V280000·2026-05-01

    2026 Ram ProMaster Recalled for Incomplete Rear Seat Assembly

    Braun Corporation is recalling 2026 Ram ProMaster vehicles because the rear bench seat may be missing two legs, which could fail to restrain occupants in a crash.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V281000·2026-05-01

    Mercedes-Benz vehicles recalled over instrument panels that go blank

    Mercedes-Benz USA is recalling 144,049 vehicles because the infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH GLC 300, GLC 300 4MATIC, C 300 4MATIC, E 450 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide