Recall Z-0113-2018— Medline Industries Inc
Class II · Terminated
Class II FDA medical device recall by Medline Industries Inc, initiated 2017-10-10, terminated 2020-08-04. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER, 21.3 in (54 cm) FOR ENDOTRACHEAL TUBE, 12 Fr, REF DYNCSDS12, 1 Each, Sterile. Reason: Products labeled as sterile were distributed prior to sterilization.
- Recalling firm
- Medline Industries Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-10-10
- Terminated
- 2020-08-04
- Firm location
- Northfield, IL, United States
Product description
MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER, 21.3 in (54 cm) FOR ENDOTRACHEAL TUBE, 12 Fr, REF DYNCSDS12, 1 Each, Sterile
Reason for recall
Products labeled as sterile were distributed prior to sterilization
Data sourced from openFDA. This site is unofficial and independent of the FDA.