Utah recalls

Asteria Health testosterone pellets (200 mg) may contain metal particulate matter due to a manufacturing issue. The FDA has classified this as a Class II recall affecting multiple lot numbers distributed nationwide. No injuries have been reported to date.

Asteria Health is recalling certain testosterone pellet injections because they may contain metal particulate matter. The contamination was identified in seven specific manufacturing lots with expiration dates between June 2026 and September 2026. No injuries have been reported so far.

Asteria Health is recalling testosterone pellets (87.5 mg) because they may contain metal particles. The recall affects three specific lots distributed nationwide. No injuries have been reported so far.

Asteria Health testosterone pellets (62.5 mg) may contain metal particulate matter. The affected lot (251000125, expiring 06/02/2026) was distributed nationwide. About 1,758 pellets are involved in this recall.

Asteria Health testosterone pellets may contain metal particulate matter as a result of a manufacturing issue. The recall affects specific lot numbers distributed nationwide. No injuries have been reported to date.

Asteria Health's testosterone pellets may contain metal particulate matter due to a manufacturing issue. The FDA has identified five affected lot numbers distributed nationwide. No injuries have been reported.

Asteria Health testosterone pellets (25 mg) may contain metal particulate matter due to a manufacturing issue. The FDA has classified this as a Class II recall affecting multiple lot numbers distributed nationwide. No injuries have been reported to date.

Asteria Health is recalling testosterone pellets (18.0 mg, lot #251000126, expiring 06/03/2026) because they may contain metal particulate matter. The recall affects 146 pellets distributed nationwide. No injuries have been reported.

Asteria Health testosterone pellets (12.5 mg) may contain metal particulate matter due to a manufacturing issue. The recall affects specific lots distributed nationwide. No injuries have been reported to date.

Asteria Health's estradiol 37.5 mg sterile pellets may contain metal particulate matter. This affects lot 253000125, expiring 06/09/2026. No injuries have been reported to date.

Asteria Health estradiol 25 mg pellets may contain metal particulate matter. The affected lot (253000136, expiring 07/01/2026) was distributed nationwide. No injuries have been reported.

Asteria Health is recalling estradiol 22 mg pellets (Lot# 253000126, expiring 06/09/2026) because they may contain metal particulate matter. The recall affects 133 pellets distributed nationwide. No injuries have been reported.

Asteria Health's estradiol 20 mg hormone pellets may contain metal particulate matter. This affects one specific lot (253000124) with an expiration date of June 2, 2026, distributed nationwide. No injuries have been reported.

Asteria Health is recalling estradiol pellets (18 mg) because some may contain metal particulate matter. The affected lot was distributed nationwide. No injuries have been reported.

Asteria Health estradiol 15 mg pellets may contain metal particulate matter, a foreign substance that could pose a health risk. The FDA has identified four affected lot numbers distributed nationwide. No injuries have been reported to date.

Asteria Health estradiol pellets (12.5 mg) may contain metal particulate matter. The affected lots were distributed nationwide. No injuries have been reported to date.

Asteria Health is recalling estradiol hormone pellets (10 mg) because they may contain metal particles. The affected pellets were distributed nationwide. No injuries have been reported so far.

Presence of Foreign substance - potential presence of metal particulate matter

Unichem Pharmaceuticals distributed 60,000 tablets of Doxazosin 4 mg with incorrect imprinting on the tablets themselves. This labeling error could cause confusion about the medication's identity and strength. The affected lot is GDSH25006, which expires in August 2027.

Pro Numb Tattoo Numbing Spray (4% Lidocaine) in lot J15 was distributed nationwide but did not meet FDA manufacturing standards. The spray may not be safe or effective as a result.

Pro Numb Tattoo Numbing Spray (5% lidocaine) is being recalled due to manufacturing quality control issues. The FDA found that the product was not made under proper conditions. Certain lot numbers (J01–J14 and J55–J69) distributed nationwide may be affected.

Hydromassage rotary jets in Watkins Highlife Collection spas can create strong suction that may entangle a user's hair and pull their head underwater. One incident of hair entanglement has been reported. The recall affects 2023–2025 models including Grandee, Envoy, Vanguard, Aria, Prodigy, Sovereign, Jetsetter, and Jetsetter LX spas.

Beloems model BL-BR201 portable bed rails can trap users between the rail and mattress, creating a risk of suffocation. The rails also fail safety standards for stability and secure attachment, and have incorrectly sized pins that can cause cuts.

CheerKid-branded baby bath seats (Model BH-222) can tip over during use because they are unstable, creating a serious risk of drowning. The seats do not meet safety standards for infant bath seats. About 590 units were sold on Amazon starting in September 2025.

Fortemotus Direct adult portable bed rails (model USFTMTJAS008) can trap users between the rail and mattress, creating a serious risk of asphyxiation and death. The rails also fail safety standards for stability and retention, and have incorrectly sized pins that can cause cuts.

SOOWERY 6-drawer dressers can tip over and trap children if not anchored to the wall, creating a serious injury or death risk. About 166 dressers were sold online through Amazon from December 2025 to January 2026. The dressers do not meet federal safety standards for furniture stability.

LShome brand smoke detectors sold on Amazon may fail to sound an alarm during a fire if their internal sensor settings are incorrect. This creates a serious risk that you won't be warned in time to escape a fire.

The mounting bolt on ETAC Molift 4-point sling bars (models 1430116, 1430117, 1430115) can break during assembly or use due to material deformation at the joint. This can cause the lifting bar to lose proper function, affecting the safety and reliability of the mobile hoist. About 25 units have been distributed worldwide.

The mounting bolt on Molift 2-point sling bars (models 1530101 and 1530102) can break during assembly or use due to material deformation. This can limit the joint's movement and prevent the hoist from working properly. No injuries have been reported.

The bolt that connects the lifting bar to the arm on certain Molift Mover 300 hoists can break due to material deformation in the joint. This can cause the lifting mechanism to become immobile and stop working properly, creating a safety risk during patient transfers.