MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C
Reported: February 7, 2024 Initiated: December 21, 2023 #Z-0968-2024
Product Description
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C
Reason for Recall
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 4200 units
- Distribution
- US Nationwide distribution.
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 4200 units.
Why was this product recalled? ▼
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 7, 2024. Severity: Moderate. Recall number: Z-0968-2024.
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