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.

Which agencies issued them

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.

2551–2575 of 85308

SevereFDA (Devices)·Z-1719-2026·2026-04-15
Medline non-vascular and vein packs recalled over syringe adaptor defect
Medline is recalling Non Vascular Pack and Vein convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1729-2026·2026-04-15
Medline TAVR procedure packs recalled over syringe adaptor disconnection risk
Medline is recalling TAVR PACK convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 108 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: TAVR PACK, Medline SKU # DYNJ84472
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1716-2026·2026-04-15
Medline cath lab packs recalled over syringe rotating adaptor disconnection
Medline is recalling cath lab and angiography procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 17,902 kits are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CATH LAB PACK-LF, Medline SKU 00-HCT055P; 2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q; 3. ANGIOGRAPHY CATH LAB,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1722-2026·2026-04-15
Medline laparoscopic and minor procedure packs recalled over syringe adaptor defect
Medline is recalling laparoscopic herniorrhaphy, lap and minor procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. LAPAROSCOPIC HERNIORRHAPHY DSC, Medline SKU # DYNJ63021B; 2. LAP PACK, Medline SKU # DYNJ64297B; 3. MINOR PROCEDURE PACK, Medl
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1728-2026·2026-04-15
Medline robotic surgery packs recalled over syringe adaptor unwinding risk
Medline is recalling Robotic Pack and Uro/Gen Robotic Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1713-2026·2026-04-15
NAMIC angiographic control syringes recalled over rotating adaptor unwinding
Medline is recalling NAMIC Angiographic Control Syringes because the rotating adaptor can unwind during use, causing a loose connection or full disconnection from the manifold. 192,690 units are affected.
Product
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1724-2026·2026-04-15
Medline cardiac catheterization kits recalled over syringe adaptor unwinding
Medline is recalling right and left heart catheterization and angiography kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 79,843 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. MTS RH LFT HRT KIT, Medline SKU # 60010508; 2. MTS 3V W/GUIDE, Medline SKU # 60100701; 3. ANGIOGRAPHY KIT, Medline SKU # 60131
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1721-2026·2026-04-15
Medline head, neck and heart cath packs recalled over syringe adaptor defect
Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K; 2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 3. HEART CATH PACK-LF, Medlin
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1714-2026·2026-04-15
Medline CVOR angiography packs recalled over syringe adaptor unwinding risk
Medline is recalling CVOR Angiography Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 3,120 kits are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1720-2026·2026-04-15
Medline special procedure trays recalled over syringe adaptor disconnection risk
Medline is recalling Special Procedure Trays containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 762 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1727-2026·2026-04-15
Medline delivery packs recalled over syringe rotating adaptor disconnection risk
Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1715-2026·2026-04-15
Medline custom manifold kits recalled over syringe adaptor unwinding risk
Medline is recalling custom manifold and cryo EP manifold kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 1,698 kits are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061; 2. CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074; 3. CRYO EP MANIFOLD KIT, M
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1730-2026·2026-04-15
Medline arthroscopy and extremity packs recalled over syringe adaptor unwinding
Medline is recalling Shoulder Arthroscopy and Extremity Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. SHOULDER ARTHROSCOPY PACK, Medline SKU # DYNJ30880M; 2. EXTREMITY PACK, Medline SKU # DYNJ64295A.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1723-2026·2026-04-15
Medline minor plastic surgery packs recalled over syringe adaptor unwinding risk
Medline is recalling Minor Plastic-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0432-2026·2026-04-15
Sodium Chloride Injection Recalled Due to Lack of Assurance of Sterility
Fresenius Kabi USA, LLC is recalling certain batches of 0.9% Sodium Chloride Injection due to concerns regarding sterility assurance.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1795-2026·2026-04-15
Preeclampsia growth factor assay recalled over out-of-range quality control values
B.R.A.H.M.S PlGF Plus KRYPTOR in vitro diagnostic tests are being recalled after customers observed out-of-range values at the lowest quality control level, which can contribute to falsely elevated results.
Product
B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the B¿R¿A¿H¿M¿S KRYPTOR compact PLUS analyzers. in vitro diagnostic test for Placental Growth Factor
Category
Medical Device
Distribution
15 states
HighFDA (Drugs)·D-0433-2026·2026-04-15
Fresenius sodium chloride 1,000 mL dialysis-supplied bags recalled over sterility
Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP in 1,000 mL single dose freeflex bags distributed by Fresenius Medical Care RTG, citing lack of assurance of sterility.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V241000·2026-04-15
Winnebago Recalls Suncruiser and Sunflyer Motorhomes for Missing Side Reflectors
Winnebago is recalling 2027 Suncruiser and 2026-2027 Sunflyer motorhomes because side reflectors may be missing, reducing visibility to other drivers.
Product
WINNEBAGO — WINNEBAGO SUNCRUISER, SUNFLYER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0436-2026·2026-04-15
Fresenius Kabi 100 mL dextrose injection bags recalled over sterility assurance
Fresenius Kabi is recalling three batches of 5% Dextrose Injection, USP, 5 g per 100 mL in freeflex bags, citing lack of assurance of sterility.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0651-2026·2026-04-15
Zarlengo's chocolate gelato omits soy from the contains statement
Zarlengo's Chocolate Gelato is being recalled because soy lecithin appears in the ingredients statement but soy is not declared in the contains statement.
Product
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0430-2026·2026-04-15
Fresenius Kabi 100 mL sodium chloride bags for BD recalled over sterility
Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP in 100 mL single dose freeflex bags distributed by BD, citing lack of assurance of sterility.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1793-2026·2026-04-15
Multi-parameter command modules may produce inaccurate cardiac output readings
A circuit board issue in Multi-parameter Command Module model 91496 can start cardiac output measurement early in Auto mode, producing errors and inaccurate readings. 1,790 units are affected.
Product
Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0435-2026·2026-04-15
Fresenius Kabi 50 mL dextrose injection bags recalled over sterility assurance
Fresenius Kabi is recalling 5% Dextrose Injection, USP, 2.5 g per 50 mL supplied in 100 mL freeflex bags, citing lack of assurance of sterility.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0650-2026·2026-04-15
Zarlengo's Chocolate Chocolate Chip Gelato Recalled for Undeclared Soy Allergen
Zarlengo Italian Ice is recalling Chocolate Chocolate Chip Gelato in multiple sizes because soy lecithin is listed in the ingredients but soy is not declared in the allergen statement, posing a risk to consumers with soy allergies.
Product
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminat
Category
Food
Distribution
3 states
HighFDA (Food)·H-0652-2026·2026-04-15
Zarlengo's Double Dark Chocolate Gelato recalled for undeclared soy allergen
Zarlengo Italian Ice is recalling Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets because soy lecithin is listed in the ingredients but soy is not disclosed in the allergen statement, posing a risk to consumers with soy allergies.
Product
Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Category
Food
Distribution
3 states