Recall Z-2911-2020— C.A. Greiner & Sohne Gesellschaftmbh
Class II · Ongoing
Class II FDA medical device recall by C.A. Greiner & Sohne Gesellschaftmbh, initiated 2020-07-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.. Reason: Sample leaking from the sleeve covering the needle inside the cannula.
- Recalling firm
- C.A. Greiner & Sohne Gesellschaftmbh
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2020-07-27
- Firm location
- Kremsmunster, N/A, Austria
Product description
Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.
Reason for recall
Sample leaking from the sleeve covering the needle inside the cannula
Data sourced from openFDA. This site is unofficial and independent of the FDA.