165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a...
ICU Medical de Mexico, S.A. de C.V. began a recall of 165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which... on . FDA classified it as Class II and gives the reason as "ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female...". As of , the recall status on record is Terminated.
Recall record
- Recall number
- Z-2798-2018
- Classification
- Class II
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- ICU MEDICAL de MEXICO, S. de R.L. de C.V.
- Product
- 165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system.
- Product code
- FMG Stopcock, I.V. Set
- Reason for recall
- ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.
- FDA root cause
- Other
- Action
- ICU Medical notified customers of the recall on about 03/01/2018 via URGENT: Medical Device Recall Notification. The notification informed customers that this was an update and expansion to previously initiated recall. Instructions included to inspect inventory for affected devices, arrange for the return of affected devices, and complete and return the Urgent Medical Device Recall Notification Response Form to [email protected].
- Quantity in commerce
- 50 pouches
- Distribution
- US distribution to AZ, MA, NC, OH, TX, VA, WA. Worldwide distribution to Belgium, France, Germany.
- Product codes and lots
- Item Number 011-AM3003. Lot Number 3297342, UDI Number (01) 1 0840619 09275 1 (17) 210700 (30) 50 (10) 3597342, Expiration Date 07/01/2021.
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-2797-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2798-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2799-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2800-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2801-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2802-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2803-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2804-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2805-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2806-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2807-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2808-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2809-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2810-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2811-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2812-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2813-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2814-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2815-2018 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2816-2018 | Class II | Terminated | Voluntary: Firm initiated |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
