State

Texas product recalls

73,106 recalls have nationwide distribution and so reach Texas. 12,428 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,428
Critical: 1,720
Severe: 2,422
Most recent: 2026-10-02

Of the 12,428 recalls naming Texas we have scored against our rubric, 1,720 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,422 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,428 recalls whose distribution notice names Texas specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12226–12250 of 85534

HighFDA (Food)·F-1294-2024·2024-06-12
Blueberry Cream Cheese Spread recalled for potential Salmonella
Schreiber Foods Inc is recalling 835,721 units of Essential Everyday Blueberry Cream Cheese Spread (8 oz) due to potential Salmonella contamination. No illnesses have been reported.
Product
Blueberry Cream Cheese Spread, Net Wt. 8 oz. (226g). Keep Refrigerated, packaged under the brand Essential Everyday, UPC 0 41303-04876 4. Distributed By UNFI, Providence, RI 02908.
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1969-2024·2024-06-12
Vascular graft component separation: Atrium Medical ADVANTA VXT recall
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider mechanism from the core component, which could compromise device integrity.
Product
ADVANTA VXT, 7X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1972-2024·2024-06-12
Vascular Graft Component Separation Risk in ADVANTA VXT Models
Atrium Medical Corporation recalled 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Patients should consult their healthcare provider regarding appropriate follow-up care.
Product
ADVANTA VXT, 7X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1292-2024·2024-06-12
Strawberry Cream Cheese Spread Recalled for Potential Salmonella Contamination
Schreiber Foods Inc is recalling Strawberry Cream Cheese Spread sold under brands including Fareway, Happy Farms, Hy-Vee, and Schnuck due to potential Salmonella contamination. Approximately 835,721 units were distributed across multiple states and Puerto Rico.
Product
Strawberry Cream Cheese Spread, Net Wt 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83052 2. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Happy Farms, UPC 4099100 101744, Dist & Sold Exclusively by Aldi, Batavia, IL…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1935-2024·2024-06-12
LOSPA Patella Knee Component Recalled for Unsupported Expiration Date
CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.
Product
LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description: Patella
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1999-2024·2024-06-12
Vascular Graft Swivel Rod Separation Reported in ADVANTA VXT Devices
Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.
Product
ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1986-2024·2024-06-12
Vascular graft component separation reported in Advanta VXT devices
Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.
Product
ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1937-2024·2024-06-12
Medline Disposable Syringes Recalled for Inaccurate Volume Delivery
Medline is recalling 25.2 million Luer Lock disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity. The inaccuracy may pose a risk to patient health.
Product
MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1993-2024·2024-06-12
Vascular graft component separation reported in ADVANTA VXT devices
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. No injuries have been reported.
Product
ADVANTA VXT, 4-6X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2013-2024·2024-06-12
FDA Recalls FLIXENE Vascular Graft Devices for Component Separation
Atrium Medical Corporation recalls FLIXENE vascular graft devices due to reported separation of the Slider GDS Swivel Rod from its core, which could affect device function.
Product
FLIXENE, 4-7X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2000-2024·2024-06-12
Vascular Graft Recalled Due to Potential Component Separation Risk
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to complaints of separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units have been distributed worldwide.
Product
ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1995-2024·2024-06-12
Vascular Graft Component Separation Recall - Atrium Medical ADVANTA VXT
Atrium Medical Corporation is recalling the ADVANTA VXT vascular graft due to reported separation of the Swivel Rod from the Swivel Core. The component separation poses a risk of device failure.
Product
ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1983-2024·2024-06-12
Vascular graft separation defect recalled by Atrium Medical
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of internal components. The defect affects over 53,000 units distributed worldwide.
Product
ADVANTA VXT, 6X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1293-2024·2024-06-12
Schreiber Foods Chive and Onion Cream Cheese Spread Recalled for Salmonella Risk
Schreiber Foods is recalling Chive and Onion Cream Cheese Spread sold under the Fareway, Happy Farms, and Hy-Vee brands due to potential Salmonella contamination. Affected consumers should not consume the product.
Product
Chive and Onion Cream Cheese Spread, Net Wt. 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83066 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Happy Farms, UPC 4099100 101751. Dist & Sold Exclusively by Aldi, Batavia, IL…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1953-2024·2024-06-12
Vascular Graft Device Recalled for Slider Component Separation
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the slider component from the swivel core. The recall affects 53,308 units worldwide.
Product
ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1989-2024·2024-06-12
ADVANTA VXT Vascular Graft Recalled for Swivel Rod Separation Risk
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts after reports of separation between the Slider GDS Swivel Rod and Swivel Core. This structural defect could affect device performance.
Product
ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2021-2024·2024-06-12
GlideScope Core 15-inch Monitor Recalled for Potential Image Loss Software Issue
Verathon is recalling GlideScope Core 15-inch monitors due to software issues causing potential image loss or degradation. Approximately 2,568 units were distributed across the US and internationally.
Product
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-2009-2024·2024-06-12
Vascular graft recalled for swivel rod separation risk
FDA recalls Atrium Medical's FLIXENE vascular grafts due to reports of the swivel rod separating from the core, potentially compromising device integrity.
Product
FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1955-2024·2024-06-12
Vascular Graft Component Separation Recall: ADVANTA VXT Slider
Atrium Medical recalls ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. The defect affects 53,308 units distributed worldwide.
Product
ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2001-2024·2024-06-12
FDA Recalls ADVANTA VXT Vascular Grafts Due to Component Separation
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts because the Slider GDS Swivel Rod may separate from the Swivel Core. A total of 53,308 units are affected.
Product
ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1991-2024·2024-06-12
Vascular graft devices subject to swivel rod separation from core assembly
Atrium Medical Corporation is recalling ADVANTA VXT vascular graft devices due to reports of the swivel rod separating from the core. The separation could compromise device function.
Product
ADVANTA VXT, 6X100, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2024·2024-06-12
Vascular graft recalled for reported swivel rod separation from core
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of the swivel rod separating from the swivel core. Patients and healthcare providers should contact the manufacturer for guidance.
Product
ADVANTA VXT, 8X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1998-2024·2024-06-12
Vascular graft recall due to slider mechanism separation defect
Atrium Medical is recalling ADVANTA VXT vascular grafts due to separation of the slider mechanism. The defect affects over 53,000 units distributed worldwide and could compromise graft function.
Product
ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1939-2024·2024-06-12
Stryker Synchro Neuro Guidewires Recalled for PTFE Coating Damage Risk
Stryker Neurovascular is recalling certain lots of Synchro Neuro Guidewires due to PTFE coating damage that can occur when using a backloading technique with the optional introducer. Clinicians should avoid the backloading technique with affected product.
Product
The Synchro Neuro Guidewires are a steerable guidewire family with a shapeable tip. The outside diameter of the Synchro 10 guidewire is 0.010in. The outside diameter of the Syncrho 14 guidewire is 0.014in. The guidewires are compatible with existing microcatheters used in common…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2007-2024·2024-06-12
FLIXENE Vascular Graft Recall for Swivel Rod Component Separation
Atrium Medical is recalling FLIXENE vascular grafts due to complaints of separation between the Swivel Rod and Swivel Core components. The recall affects 53,308 units worldwide, including 11,236 in the US.
Product
FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide