Recall Z-0828-2020
Medicrea International · initiated September 16, 2019
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
Codes / lots: Lot number(s) : 18G0368; 19H0009; 18F0138; 18G0038
Reason for recall
Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded
FDA-determined cause: Process control
Action taken
Medicrea International issued letter dated 9/12/19 to US Distributor stating reason for recall, health risk and action to take: Immediately check your internal inventory and quarantine all subject devices pending return to MEDICREA 2. Circulate this Field Safety Notice internally to all interested/affected parties. 3. Inform MEDICREA if any of the subject devices have been distributed to other organisations. Please inform MEDICREA of any adverse events concerning the use of the subject devices 2. Please comply with any local laws or regulations concerning the notification of adverseevents to your National Competent Authority. 3. Complete the attached customer response form. It may be that you no longer have any physical inventory on site. Contact: Karine TROGNEUX, MEDICREA INTERNATIONAL Regulatory Affairs Manager, Direct : +33(0)4.69.85.95.39, Standard : +33 (0)4.72.01.87.87. Fax - N +33 (0)04 72 01 87 88, Mail : ktrogneux@medicrea.com
Details
- Recall number
- Z-0828-2020
- Initiated
- September 16, 2019
- Product code
- KWP – Appliance, Fixation, Spinal Interlaminal
- Quantity
- 190 units
- Distribution
- Nationwide
- Recalling firm
- Medicrea International, Vancia Rillieux La Pape
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0827-2020 Class II | Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product reference : A06010130Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded | 09/16/2019Open, Classified |