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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:187840

Proponent pacemaker, Models: a) L200 b) L201 c) L209 d) L210 e) L211 f) L221 g) L231

Official recall number

Z-1999-2021

Evidence summary

Product code
LWP
Recall status
Open, Classified
Event initiated
June 03, 2021
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1999-2021

Field note

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