Texas recalls
4382 federal recalls on file affecting Texas - 1007 Texas-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline robotic procedure kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using recalled Medline convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline angiography kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline GLOVE PACK 7.0 medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline medical convenience kits SKU DYNJ86596
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline procedure kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline medical kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline Special Procedure Tray kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline NAMIC RA syringes immediately
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideNAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SY
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline angiographic syringes
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using recalled Medline catheter lab kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline manifold kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideMedline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using Medline NAMIC angiographic syringes
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceMedlineClass INationwideStop using affected Medline angiographic syringes
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- 2026-04-15FDA-DeviceSiemensClass IINationwideContact Siemens about your ARTIS imaging system
During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system settings and imaging conditions, as well as the applicable regulatory requirements.
- 2026-04-15FDA-FoodRiverence ProvisionsClass IIStop using Riverence Smoked Trout Dip
Label declares cream cheese but does not declare milk
- 2026-04-15FDA-FoodZarlengo Italian IceClass IICheck Zarlengo gelato for missing soy allergen label
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-FoodZarlengo Italian IceClass IIStop eating Zarlengo's Chocolate Gelato
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-FoodZarlengo Italian IceClass IIStop using Zarlengo Chocolate Chocolate Chip Gelato
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- 2026-04-15FDA-DrugTevaClass IINationwideStop using recalled Teva Clonidine patches
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTevaClass IINationwideCheck your Clonidine patch lot numbers
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTevaClass IINationwideStop using recalled Teva Clonidine patches
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugGE HealthcareClass IINationwideCheck Omnipaque injection lot numbers immediately
Presence of particulate matter
- 2026-04-15FDA-DrugGE HealthcareClass IINationwideCheck GE Healthcare Omnipaque injection lot numbers
Presence of particulate matter
- 2026-04-15FDA-DrugViatris, Inc.Class IINationwideCheck your Xanax XR 3 mg prescription bottle
Failed Dissolution Specifications
- 2026-04-15FDA-DrugPreferred Pharmaceuticals, Inc.Class IINationwideStop using Preferred Pharmaceuticals Artificial Tears
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IINationwideStop using Fagron Vancomycin HCL IV bags
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Get notified about new Texas recalls
Free weekly digest. Add Texas to your profile to filter alerts to your state.
Get the Sunday Brief