SunMed Holdings recalls

SunMed Holdings has 18 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 4 Feb 2026. 17 are still ongoing. 4 were reported in the last 12 months. The most frequent reason is packaging defects.

Total recalls18since 2022
Last 12 months4reported
Class I633% of total
Ongoing17latest 4 Feb 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 6 33%Class II 12 67%Class III 0 0%

Why sunmed holdings is recalled

By year

Ongoing sunmed holdings recalls

17 active

All sunmed holdings recalls, newest first

18 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IBroselow Pediatric Emergency Rainbow Tape recalled by SunMed HoldingsSunMed HoldingsDevice MalfunctionNationwide
DeviceCLASS IBroselow" Filled Broselow Organizer recalled by SunMed HoldingsSunMed HoldingsDevice MalfunctionNationwide
DeviceCLASS IBroselow Domestic Complete ALS Organizer recalled by SunMed HoldingsSunMed HoldingsDevice MalfunctionNationwide
DeviceCLASS IBroselow Pediatric Emergency Rainbow Tape recalled by SunMed HoldingsSunMed HoldingsDevice MalfunctionNationwide
DeviceCLASS IBroselow Pediatric Emergency Rainbow Tape (distribution by AirLife) recalledSunMed HoldingsOtherNationwide
DeviceCLASS IAdult Manual Resuscitator with Medium Adult Mask recalledSunMed HoldingsDevice MalfunctionNationwide
DeviceCLASS IIVentlab, LLC RescuMed manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IICuraplex manual resuscitators with integrated manometer recalledSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC Horizon manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC V-Care manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC SafeSpot manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC Stat-Check manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC BreathTech manual resuscitators recalled by SunMed HoldingsSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIVentlab, LLC AirFlow manual resuscitator devices recalledSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIMedline manual resuscitators with integrated manometer recalledSunMed HoldingsPackaging DefectsNationwide
DeviceCLASS IIAirQ3 Self Pressurizing ILA recalled by SunMed HoldingsSunMed HoldingsOtherNationwide
DeviceCLASS IIAir-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size recalledSunMed HoldingsOtherNationwide
DeviceCLASS IIFull Kit Pulset 3cc SyringeSafety Tip 25u BH recalled by SunMed HoldingsSunMed HoldingsSterility10 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.