Recall Z-0312-2024— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2023-11-01. FDA's recall record names no specific 510(k) clearance for this event. Product: CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562. Reason: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert..
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-11-01
- Firm location
- Northfield, IL, United States
Product description
CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.