🇺🇸·Sep 9Regulatory
Device recall: HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF: 10301016 (EU)
Official structured record identifier: 99496.
Publisher
o
openFDA Device Recalls
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- September 9, 2026
- Language
- EN
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Official structured record identifier: 99496.
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Source: openFDA Device Recalls
Scope: Regulatory
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