Connecticut recalls

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Primark sold The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets containing crayons with high levels of strontium and aluminum. If a young child ingests these crayons, it could cause poisoning. No injuries have been reported so far.

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.

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.

The fan wheel in certain NorthStar hot water pressure washers can fail, causing the burner to operate abnormally. This can produce smoke and flames during use, creating a fire hazard. The recall affects three commercial models made between January and August 2025.

These LED light sets contain coin batteries (CR2450 and CR2032) that children can easily access and swallow. Swallowing these batteries can cause serious internal burns and death. The lights also lack required safety warnings.

Mindbodygreen Ultimate Multivitamin+ bottles contain iron and are not packaged in child-resistant containers, violating federal safety requirements. Young children who swallow the contents could suffer serious injury or death from iron poisoning.

The rear wheel bolts on certain 2026 Trek FX+ and Electra Townie Go! electric bicycles can break during use, causing the rear wheel to separate from the frame. This poses a serious fall risk to riders. Trek has received seven reports of bolt breakage, though no injuries have been reported yet.

AiTuiTui Pull String Teething Toys sold on Amazon contain long string "tentacles" that children can pull off and choke on. The CPSC has received 15 reports of choking incidents and 2 reports of children biting pieces off the silicone strings. The toy does not meet federal safety standards for toys.

Sefudun 5% Minoxidil Hair Growth Serum bottles do not have child-resistant caps, as required by law. If a young child swallows the contents, it could cause serious injury or death. The product was sold on Amazon from December 2023 through August 2025.