BLOOD CULTURE KIT, REF DYNDH1647B
FDA device recall Z-0314-2024 · posted 2023-11-16 · Open, Classified
Recall details
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Reason for recall
- This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
- Action taken
- Medline Industries issued a MEDICAL DEVICE RECALL notice to its consignees on 11/01/2023 via email. The notice explained the issue and requested that the destruction of the affected kits. Consignees were also instructed to notify all parties if the kits were transferred.
- Root cause
- Under Investigation by firm
- Status
- Open, Classified
- Product code
- OIB
- Quantity affected
- 1890 kits
- Distribution
- US Nationwide distribution in the state of California.
- Date initiated
- 2023-11-01
- Date posted
- 2023-11-16
- Location
- Northfield, IL
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