Device recall: MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B; 2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A; 3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D; 4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973; 5) CHLA ECMO / CARDIAC PACK, Medline
Official structured record identifier: 98994.
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: 98994.
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Source: openFDA Device Recalls
Scope: Regulatory
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