New Mexico recalls

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.

Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.

Foreign object (stainless steel dust/flakes or shreds of plastic)

Foreign object (stainless steel dust/flakes or shreds of plastic)

Foreign object (stainless steel dust/flakes or shreds of plastic)

Foreign object (stainless steel dust/flakes or shreds of plastic)

Failed Dissolution Specifications

Presence of particulate matter: identified as Buprenorphine free base

Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.

Blackstone Products of Providence, Utah is voluntarily recalling certain lots of Blackstone Parmesan Ranch seasoning products because they have the potential to be contaminated with Salmonella. Blackstone’s action is based on a California Dairies, Inc. recall of dry milk powder due to potential Sal

The electronic start/stop button on the pressure washer can malfunction and self-start, posing a risk of serious injury or death due to carbon monoxide poisoning, if the unit is in a confined space.

The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.

The platform inside the recalled tower can loosen over time, causing it to become unstable or detach, and ultimately posing a fall hazard to young children.

The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard.

The recalled harness' D-ring can release, allowing the attachment point to open, posing a risk of serious injury or death from a fall hazard.

The recalled harnesses are missing rivets in the FAST LT PIN-LOCK buckles, causing the buckles to open, posing a risk of serious injury or death from a fall hazard.

The weight plates can fail to engage completely during weight adjustment and dislodge from the dumbbell handle when used, posing an impact hazard.

The swing seat can detach from the frame while in use, posing a risk of serious injury or death from a fall hazard.

The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under?Reese's Law.?When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

The Misco Sports Badminton Toy Sets violate the mandatory safety standard for children's toys because the shuttlecocks contain button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and deaths.

The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress and becoming a deadly choking hazard.

The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.

FOR IMMEDIATE RELEASE MUMBAI, INDIA and PRINCETON, NJ - May 13, 2026 – Sun Pharma is voluntarily recalling within the U.S. to the hospital/user level, one batch of DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL, Lot # HAG2581B, Expiration 05/2027 (675 vials). The single batch of 675 vials i