Recall Z-0123-2023— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2022-09-09. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632. Reason: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit..
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-09-09
- Firm location
- Northfield, IL, United States
Product description
MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632
Reason for recall
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
Data sourced from openFDA. This site is unofficial and independent of the FDA.