The Recall Desk

State

Texas product recalls

72,907 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.

Which agencies issued them

These figures cover only the 12,389 recalls whose distribution notice names Texas specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1076–1100 of 85296

  • SevereFDA (Devices)·Z-2452-2026·2026-07-01

    Medline Convenience Kits containing anesthesia components recalled for quality issues

    Medline Industries is recalling Medline Convenience Kits (models DYNJ905503F and DYNJ905503G) that contain Arrow Kits with Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2582-2026·2026-07-01

    Medline polycarbonate syringes recalled for unapproved design changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO CATH COMBINED PACK DYNJ43609S ANGIO PACK DYNJ67987D DYNJ80317A ANGIO SPECIAL PROCEDURE-LF DYNJ38412C ANGIOGRAM SET UP PACK DYNJ66260A ANGIOGRAPHY PACK DYNJ44293I ANGIOGRA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1117-2026·2026-07-01

    Utz Quality Foods Dirty Sour Cream Onion Potato Chips Salmonella Recall

    Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.

    Product
    2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2600-2026·2026-07-01

    Abiomed Impella CP Introducer Kit Recalled for Thrombus Risk

    Abiomed is recalling the 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP due to potential thrombus formation during prolonged use. The recall affects 17 units distributed in the United States and Japan.

    Product
    Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1099-2026·2026-07-01

    Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.

    Product
    Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1113-2026·2026-07-01

    Zapp's Brand Bayou Blackened Ranch Potato Chips Recalled for Salmonella

    Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.

    Product
    2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2454-2026·2026-07-01

    Medline Convenience Kits with Central Line Insertion recalled for quality issues

    Medline Industries is recalling two models of Convenience Kits (ACC011142 and DYNJ8407) distributed nationwide. The kits contain injectable anesthetics that were recalled due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142; 2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V422000·2026-07-01

    BMW Recalls 428 Vehicles for Integrated Brake System Malfunction

    BMW is recalling 428 vehicles from 2023-2025 due to a potential integrated brake system malfunction that may reduce braking power or disable stability controls.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE 740I XDRIVE, 740I, X1, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2601-2026·2026-07-01

    Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kits Recalled

    Abiomed is recalling certain Impella CP Set with SmartAssist (10th Generation) units with affected 14Fr Low Profile Introducer Kits due to potential for thrombus (blood clot) formation during prolonged use.

    Product
    Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1104-2026·2026-07-01

    Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.

    Product
    Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1115-2026·2026-07-01

    Utz Dirty Maui Onion Chips Recalled for Potential Salmonella

    Utz Quality Foods is recalling 2.0 oz bags of Dirty Maui Onion Chips due to potential Salmonella contamination. The product was distributed across 32 US states.

    Product
    2.0 oz Dirty Maui Onion Chip, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2590-2026·2026-07-01

    Medical Device Convenience Kits with 10mL Polycarbonate Syringes Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2558-2026·2026-07-01

    Surgify Halo 4.0mm Extendable Surgical Burr Recall for Breakage Risk

    Surgify Medical is recalling Surgify Halo 4.0 mm Extendable surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The breakage could create a safety hazard during the procedure.

    Product
    Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2453-2026·2026-07-01

    Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled

    Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2026·2026-07-01

    VOCSN+Pro Respiratory System Backup Battery Alarm Failure Recall

    Ventec Life Systems is recalling VOCSN+Pro respiratory systems due to a damaged backup battery that may prevent the backup alarm from activating during power loss, delaying caregiver awareness of a hazardous condition.

    Product
    VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1100-2026·2026-07-01

    Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars recalled

    Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.

    Product
    Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2521-2026·2026-07-01

    Da Vinci surgical system operative components with E-brake retainer pin defect

    Intuitive Surgical recalls certain Da Vinci surgical system operative components due to a defective E-brake retainer pin that may fail to engage the E-brake, potentially causing uncontrolled motion and patient injury.

    Product
    Da Vinci ASSY, PSS, SP1098, Part Number: 380601
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2553-2026·2026-07-01

    GE Healthcare AW Server Radiological Image Processing System Software Defect

    GE Healthcare is recalling the AW Server 3.2 ext. 6.5 radiological image processing system due to a software synchronization issue that may cause the wrong patient's images to be displayed without warning, potentially leading to misdiagnosis.

    Product
    GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2531-2026·2026-07-01

    Zimmer Off-Axis Alliance Glenoid Reamer Guide recalled for breakage

    Zimmer is recalling the Off-Axis Alliance Glenoid Right 4-Peg Augment Reamer Guide (Model 110040476) after five complaints that plastic guides broke during reaming.

    Product
    Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2572-2026·2026-07-01

    Surgify Halo Surgical Burr Recalled for Breakage Risk

    Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA is recalling this device nationwide due to the potential breakage hazard.

    Product
    Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2529-2026·2026-07-01

    Zimmer Off-Axis Comprehensive Shoulder System Reamer Guide Recall

    Zimmer, Inc. is recalling the Off-Axis Comprehensive Shoulder System reamer guides (Model 110040242) due to plastic guides that can catch and break during reaming. Five complaints have been received.

    Product
    Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2566-2026·2026-07-01

    Surgify Halo Spinal Surgery Burrs Recalled for Breakage Risk

    Surgify Medical is recalling Surgify Halo 5.4 mm Short burrs (Model 54.070.NVG.H1) due to potential breakage during bi-portal endoscopic spinal surgery. The hazard could affect patient safety during the procedure.

    Product
    Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2569-2026·2026-07-01

    Surgify Halo Surgical Burrs Subject to Potential Breakage Recall

    Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA has classified this as a Class II recall affecting devices distributed nationwide.

    Product
    Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.U1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2563-2026·2026-07-01

    Surgify Halo surgical burr recalled for potential breakage during spinal surgery

    Surgify Halo 40 mm surgical burrs are being recalled because they may break during bi-portal endoscopic spinal surgery, potentially creating risks during the procedure.

    Product
    Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide