191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext Set w/6-Port NanoClave Manifold w/2 Red Rings, Check...
ICU Medical de Mexico, S.A. de C.V. began a recall of 191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext Set w/6-Port NanoClave Manifold w/2 Red Rings, Check Valve, 2 MicroClave Clear, Clamp, Rotating Luer 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-2807-2018
- Classification
- Class II
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- ICU MEDICAL de MEXICO, S. de R.L. de C.V.
- Product
- 191 cm (75") Appx 2.9 ml, PVC/PUR Smallbore Bifuse Ext Set w/6-Port NanoClave Manifold w/2 Red Rings, Check Valve, 2 MicroClave Clear, Clamp, Rotating Luer.
- 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-AM6125. Lot Number 3424313, UDI Number (01) 1 0840619 09486 4 (17) 220301 (30) 50 (10) 342313, Expiration Date 03/01/2022
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.
