FDA recall notice
Emergency Response Safety Kit Recall: Airlife Removes Certain Broselow Pediatric Emergency…
FDA Recall Confirmed · Broselow Rainbow Tape · posted Feb 11, 2026
Key facts
| Notice | Emergency Response Safety Kit Recall: Airlife Removes Certain Broselow Pediatric Emergency Rainbow Tapes and Broselow ALS Organizers |
|---|---|
| Device type | Broselow Rainbow Tape |
| Status | Recall Confirmed |
| Posted | Feb 11, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- 1–9 Recall events referenced
- 1–9 UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: