🇺🇸·Sep 9Regulatory
Device recall: Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01; 3) ANEURYSM PACK, Model/Item Number (kit) BPAY14-01; 4) SPINE PACK, Model/Item Number (kit) HSLM53-01; 5) ANTERIOR CERVI
Official structured record identifier: 99469.
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: 99469.
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Source: openFDA Device Recalls
Scope: Regulatory
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