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BROSELOW™

AIRLIFE · Model 7730MOD · UDI-DI 10889483589212

OKI Prescription
0
510(k) clearances
28
Adverse events (1 deaths)
6
Recalls
12
Facilities

Description

Broselow Complete Set of Colored Pouches

Recalls

DateFirmReason
2026-09-24Cardinal Health 200, LLCKits contain infusion sets which were recalled for performance issues.
2025-12-15SunMed Holdings, LLCProduct contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
2025-12-15SunMed Holdings, LLCProduct contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
2025-12-15SunMed Holdings, LLCProduct contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
2025-12-15SunMed Holdings, LLCProduct contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
2025-05-15SunMed Holdings, LLCThe impacted tape was manufactured with incorrect information on the tape. Incorrect values are printed in the Red zone, Orange zone, and Grey zone. Using the incorrect values in t

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.