MEDLINE INDUSTRIES, LP Northfield 24 BLOOD CULTURE KIT, REF DYNDH1632 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
24 BLOOD CULTURE KIT, REF DYNDH1632
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
UDI/DI 40193489916141 (case), 10193489916140 (unit): Lot Numbers: 23EMF710, 23DMF154, 23DMA779
Products Sold
UDI/DI 40193489916141 (case), 10193489916140 (unit): Lot Numbers: 23EMF710, 23DMF154, 23DMA779
MEDLINE INDUSTRIES, LP Northfield is recalling 24 BLOOD CULTURE KIT, REF DYNDH1632 due to This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026