Every recall we track for SunMed Holdings, LLC — 18 in all — plus the complaints and injury reports the public filed about them.
SunMed Holdings recalls Broselow Pediatric Emergency Rainbow Tape model 7700REA due to potential dosing errors for Vecuronium, Flumazenil, and Ketamine. Affected units sold with specific lot numbers.
SunMed Holdings recalls Broselow Filled Organizers (model 7730IALS) due to potential dosing errors for Vecuronium, Flumazenil, and Ketamine. Affected units may cause harmful medication doses in pediatric emergencies.
SunMed Holdings recalls Broselow Domestic Complete ALS Organizer software (model 7730ALS) due to potential dosing errors for Vecuronium, Flumazenil, and Ketamine. Affected units sold with specific lot numbers.
SunMed Holdings recalls Broselow Pediatric Emergency Rainbow Tape model 7700RE due to potential dosing errors for Vecuronium, Flumazenil, and Ketamine. Affected units include specific lot numbers.
SunMed Holdings recalls AirLife Broselow Pediatric Emergency Rainbow Tape (2025 Edition) due to incorrect dosage values printed on the tape, which could cause serious harm like cardiac arrest or burns if used improperly.
SunMed recalls adult resuscitators with medium masks that have B/V filters incorrectly attached to patient ports. This may cause delays in resuscitation, leading to hypoxia or death. Affected lots include specific serial numbers.
SunMed Holdings recalls RescuMed manual resuscitators with integrated manometers due to a backwards leak causing CO2 rebreathing. Affected models include adult, infant, and pediatric resuscitators with specific serial numbers and production dates.
SunMed recalls Curaplex manual resuscitators with integrated manometers due to a backwards leak causing CO2 rebreathing. Affected models include Adult, Child, and Infant BVMs with specific reference numbers and production dates.
SunMed Holdings recalls Horizon manual resuscitators with integrated manometers due to a backwards leak causing CO2 rebreathing. Affected models include adult, infant, and pediatric versions with specific serial numbers and production dates.
Recall of Ventlab V-Care manual resuscitators with integrated manometer due to CO2 rebreathing hazard in patient valve. Affected models include Child, Infant, Pediatric and Small Adult Resuscitators with specific reference numbers.
Ventlab SafeSpot manual resuscitators with integrated manometer have a backwards leak causing CO2 rebreathing. Affected models include SafeSpot Infant Resuscitators and Safe Spot Bag with specific serial numbers. Recalled due to risk of rebreathing CO2 during resuscitation.
SunMed Holdings recalls Ventlab STAT-Check manual resuscitators with integrated manometers that can cause CO2 rebreathing due to a backwards leak in the patient valve. Affected models include Adult, Infant, and Pediatric Resuscitators with specific reference numbers and production dates.
Ventlab BreathTech manual resuscitators with integrated manometers risk CO2 rebreathing due to a backwards leak. Affected models include adult, child, infant and pediatric resuscitators with specific reference numbers and production dates.
Recalled Ventlab AirFlow manual resuscitators with integrated manometers have a backwards leak allowing CO2 rebreathing. Affected models include Adult, Child, Infant, Pediatric, and Small Adult Resuscitators with specific reference numbers. Stop using immediately to prevent potential CO2 buildup.
Medline manual resuscitators with integrated manometers have a backwards leak causing CO2 rebreathing. Affected models include adult, infant, and pediatric resuscitators with specific serial numbers. Stop using immediately to prevent potential health risks.
SunMed recalls AirQ3 Self-Pressurizing ILA devices due to incorrect gastric tube size labeling. This mismatch may prevent proper catheter insertion, requiring smaller tubes in some cases.
SunMed recalls Air-Q3 Standard ILA devices with manual cuff inflation due to inconsistent gastric tube size labeling, potentially causing improper catheter insertion.
SunMed recalls Full Kit Pulset 3cc Syringes with non-sterile spare needles that could cause skin infections or sepsis if used. Affected units include specific lot numbers and reference codes.
