Device recall: TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
Official structured record identifier: 99080.
Publisher
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- June 24, 2026
- Language
- EN
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Official structured record identifier: 99080.
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Source: openFDA Device Recalls
Scope: Regulatory
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