Texas recalls
3,725 federal recalls affecting Texas in the last 12 months - 367 Texas-specific plus 3,358 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Genesis Dual Thread Screw-In Anchor
Aju Pharm Co., Ltd. is recalling Genesis Dual Thread Screw-In Anchor devices (Models 10N47502 and 10N55002) due to reports of failure during use. The anchor may break, bend, pull out, or cause the suture to break.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Genesis Screw-In Anchor devices
Aju Pharm Co., Ltd. is recalling Genesis Screw-In Anchor devices due to reports of failure, including anchor breakage, bending, pull-out, suture breakage, and packaging damage. The recall affects models 10B45003, 10B55003, and 10B65003 distributed nationwide in California and Puerto Rico.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm Fixone Biocomposite Anchor
Aju Pharm's Fixone Biocomposite Anchor has been recalled due to reports of device failure, including anchor breakage, bending, pulling out, suture breakage, and packaging damage. The recall affects 1,088 units distributed in California and Puerto Rico. No injuries have been reported to date.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm Fixone Hybrid Anchor
Aju Pharm's Fixone Hybrid Anchor, a surgical device, has been recalled due to reports of device failure. Problems include the anchor breaking, bending, or pulling out during use, as well as suture breakage and packaging damage. This affects 233 units distributed in California and Puerto Rico.
- 2026-02-04FDA-DeviceCerapedicsClass IINationwideCheck Cerapedics PearMatrix P-15 expiration dates
Cerapedics recalled PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) due to an incorrect expiration date on certain units. The affected lot is 7014819. No injuries have been reported.
- 2026-02-04FDA-DeviceElektaClass IINationwideCheck your Elekta radiation therapy system
Elekta medical linear accelerators used in cancer radiation therapy have a manufacturing defect affecting electrical grounding in certain models and lot codes. The issue could potentially affect the safe operation of these systems. No injuries have been reported to date.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using affected Broselow Tape units
The Broselow Tape, a tool used in pediatric emergency care to determine medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given in emergency situations. The affected units have specific lot numbers and are distributed in the US, Canada, Hong Kong, and Singapore.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using Broselow ALS Organizer model 7730ALS
The Broselow Tape, a tool used in pediatric emergency care to determine correct medication doses based on a child's length and weight, contains dosing errors for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to incorrect doses being given during emergency treatment.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using affected Broselow emergency tape
SunMed Holdings is recalling certain Broselow Pediatric Emergency Rainbow Tapes because they contain incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong drug doses during pediatric emergency care. This is a serious safety issue affecting emergency departments and medical facilities.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using SunMed Broselow emergency tape
The Broselow Tape, a tool used in pediatric emergencies to calculate medication doses based on a child's length and weight, contains incorrect dosing information for three medications: Vecuronium, Flumazenil, and Ketamine. These errors could lead to wrong doses being given during emergency care. The FDA has classified this as a Class I recall, the most serious category.
- 2026-02-04FDA-FoodWeaver's BrewClass IIStop drinking Goldenroot Ginger Beer
Goldenroot Yuzu Ginger Lemongrass Ginger Beer (12 oz bottles) may contain ginger juice that was not properly pasteurized. Unpasteurized juice can harbor harmful bacteria. The recall affects bottles with use-by dates up to June 14, 2026, distributed in Texas and California.
- 2026-02-04FDA-FoodWeaver's BrewClass IIStop drinking Weaver's Brew Goldenroot Ginger Beer
Weaver's Brew Goldenroot Lemon Ginger Jalapeno Ginger Beer (12 oz bottles) may contain ginger juice that was not properly pasteurized. Unpasteurized juices can carry harmful bacteria. The affected products have use-by dates up to June 14, 2026, and were distributed in Texas and California.
- 2026-02-04FDA-FoodWeaver's BrewClass IIStop drinking Weaver's Brew Goldenroot Ginger Beer
Weaver's Brew Goldenroot Lemon Ginger Hibiscus Ginger Beer (12 oz bottles) may contain ginger juice that was not properly pasteurized. Unpasteurized juice can harbor harmful bacteria. Products with use-by dates through June 14, 2026, are affected.
- 2026-02-04FDA-FoodWeaver's BrewClass IIDon't drink Weaver's Brew Goldenroot Ginger Beer
Weaver's Brew Goldenroot Lemon Double Ginger Ginger Beer (12 oz bottles) may contain ginger juice that wasn't properly pasteurized. This could allow harmful bacteria to grow. The recall affects bottles with use-by dates up to June 14, 2026, sold in Texas and California.
- 2026-02-04FDA-FoodWeaver's BrewClass IIStop drinking Goldenroot Ginger Beer
Goldenroot Lemon Ginger Elderberry Ginger Beer may contain ginger juice that was not properly pasteurized, which can allow harmful bacteria to grow. The affected 12 oz. bottles have use-by dates up to June 14, 2026, and were distributed in Texas and California.
- 2026-02-04FDA-FoodSuperfoodsClass INationwideStop using Live it Up Super Greens powder
Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported to date.
- 2026-02-04FDA-FoodSuperfoodsClass INationwideStop using Live it Up Super Greens powder
Live it Up brand Super Greens dietary supplement powder may be contaminated with Salmonella Typhimurium. The contamination affects specific lot codes beginning with the letter "A" and expiration dates from August 2026 through January 2028. No illnesses have been reported so far.
- 2026-02-04FDA-FoodPlant Based InnovationsClass IIDon't eat HIGHER HARVEST coconut yogurt
HIGHER HARVEST by H-E-B strawberry coconut yogurt (5.3 oz) may contain undeclared almonds. The product label does not list almonds as an ingredient. This poses a serious risk to anyone with a tree nut allergy.
- 2026-02-04FDA-FoodQuten Research InstituteClass IIStop using Qunol turmeric capsules
Qunol Extra Strength Turmeric Capsules (1000mg) in 60-count and 120-count bottles have been recalled due to mold contamination in raw materials used to make the product. The contamination was found in material lots produced in July. No injuries have been reported.
- 2026-02-04FDA-DrugNovadozClass IIINationwideStop using recalled Novadoz glycopyrrolate solution
Novadoz Pharmaceuticals is recalling specific lots of glycopyrrolate oral solution (1 mg/5 mL) because the medication failed quality testing for impurities and degradation. The affected lots may not meet safety and effectiveness standards. Three lots are involved, with expiration dates between April and May 2027.
- 2026-02-04FDA-DrugGreenstoneClass IINationwideStop using Greenstone methylprednisolone Dosepak
Greenstone LLC is recalling methylprednisolone 4 mg Dosepak tablets (Lot #LG7675, expiring November 2026) because the blister foil is oriented incorrectly. This misalignment can make the dosing directions on the foil confusing or unclear, which could lead to taking the wrong dose.
- 2026-02-04FDA-DrugHaleonClass IIINationwideCheck your Parodontax mouthwash lot number
Some bottles of Parodontax Active Gum Health mouthwash (mint, 16.9 FL OZ) may be missing or have illegible lot and expiration date codes. This makes it impossible to know when the product expires. The affected lot is #0665363 with an expiration date of 08/31/2027.
- 2026-02-04FDA-DrugBaxterClass IINationwideStop using Baxter Sterile Water for Irrigation
Baxter Healthcare's Sterile Water for Irrigation 250 mL bottles may contain small plastic particles that came loose from the bottle rim and entered the solution. This affects lot G171359 with an expiration date of 05/31/2027. No injuries have been reported.
- 2026-02-04CPSCMameixNationwideStop using Scepter B62 fuel containers
Scepter B62 fuel containers lack required safety devices to prevent flash fires and have non-child-resistant spouts that can cause burns or poisoning. These red containers with yellow spouts were sold online from August 2024 through May 2025.
- 2026-02-03USDAClass INationwideDo not consume Mays Chemical frozen pork loins
Mays Chemical Company of Puerto Rico recalled approximately 46,315 pounds of frozen, raw pork boneless loins because they were imported into the United States without required reinspection. The pork was distributed to restaurants, institutions, and food service establishments in Puerto Rico. No illnesses have been reported.
- 2026-01-29CPSCGazelleNationwideStop using Gazelle Urban Arrow e-bikes
The buckle on the cargo area bench of these e-bikes can fail to fully latch, which could allow children to fall or shift unsafely during riding. Gazelle USA has received three reports of buckles not latching properly, though no injuries have been reported yet.
- 2026-01-29CPSCBazic ProductsNationwideStop using Bazic Silicone Glue immediately
Bazic Silicone Glue contains methanol but does not have child-resistant packaging required by law. The bottle is not safe from young children and could cause serious injury or death if swallowed. The label is also incorrect, falsely claiming the product is non-toxic and omitting flammability warnings.
- 2026-01-29CPSCRunshuNationwideStop using Viofairy Hair Growth Serum immediately
Viofairy Hair Growth Serum bottles contain minoxidil, a medication that must be in child-resistant packaging by law. These bottles have regular caps that children can open, creating a serious poisoning risk if swallowed. The product was sold on Amazon from January 2024 through September 2025.
- 2026-01-29CPSCStarmatrixNationwideStop using Sunneday and Blue Bay pools
Certain Sunneday and Blue Bay above-ground pools have a compression strap around the outside that can create a foothold, potentially allowing children to climb into the pool unsupervised. This drowning risk exists even if the ladder is removed. No injuries have been reported.
- 2026-01-29CPSCHobby LobbyNationwideStop using Hobby Lobby plush toys with clips
The legs on these Hobby Lobby plush toys can detach from the body, releasing small beads inside. Young children could choke on these beads. One incident has been reported, but no injuries so far.
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