FDA Device Intelligence
HomeDevice types › NZD

Stretcher, Patient Restraint

FDA product code NZD · Class 1 · General Hospital

35
Registered devices
3
Adverse events
2
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-03-10Ferno-Washington IncOn March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm invest
2016-03-10Ferno-Washington IncOn March 9, 2016, the firm was contacted regarding the possibility of incorrect labeling on the outside poly- bag of the traction splint straps. The firm inves

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.