SunMed Holdings Recalls

4 recalls found for SunMed Holdings. Check if any of your products are affected.

HIGHFDA DEVICE

Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer

Broselow recalled 384 units of their Domestic Complete ALS Organizer on December 15, 2025, due to harmful dosing errors. The recalled product affects dosages for Vecuronium, Flumazenil, and Ketamine. Healthcare providers and patients must stop using the device immediately.

SunMed Holdings
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HIGHFDA DEVICE

Broselow Pediatric Emergency Tape Recalled Over Dosing Errors

SunMed Holdings recalled 20,583 units of Broselow Pediatric Emergency Rainbow Tape on December 15, 2025. The product contains harmful dosing errors for critical medications including Vecuronium, Flumazenil, and Ketamine. Healthcare providers and patients must stop using the tape immediately and follow recall instructions.

SunMed Holdings
Product contains
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HIGHFDA DEVICE

SunMed Recalls Broselow Pediatric Emergency Tape Over Dosing Errors

SunMed Holdings recalled 95,300 units of Broselow Pediatric Emergency Rainbow Tape on December 15, 2025. The tape contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. Patients and healthcare providers must stop using the product immediately.

SunMed Holdings
Product contains
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Brand Statistics

Total Recalls
4
Pages
1