| | Class 2 Device Recall BOMImed Reusable Integrated Fiber Optic Laryngoscope Blades |  |
| Date Initiated by Firm | December 08, 2010 |
| Date Posted | May 03, 2012 |
| Recall Status1 |
Terminated 3 on May 08, 2012 |
| Recall Number | Z-1488-2012 |
| Recall Event ID |
61464 |
| Product Classification |
Laryngoscope, nasopharyngoscope - Product Code EQN
|
| Product | BOMImed Reusable Integrated Fiber Optic Laryngoscope Blades, MacIntosh and Miller styles - all sizes. Instrument is used to aid with intubation. |
| Code Information |
Lot Numbers 0310, 0510, 2710, 3210, 4010 & 4510 |
| FEI Number |
3005396516
|
Recalling Firm/ Manufacturer |
Bomimed Inc 96 Terracon Pl Winnipeg Canada Manitoba
|
| For Additional Information Contact | Trina Friesen 204-633-2664 Ext. 234 |
Manufacturer Reason for Recall | On 9/1/2010 BOMImed, Inc. Winnipeg, MB, Canada initiated a recall of their BOMImed Integrated Reusable Laryngoscope Blades (Macintosh & Miller styles - all sizes), Model #OL-32D0 to OL-32D4 & OL-32E00, OL-32E0, OL-32E1, OL-32E2, OL-32E3, OL-32E4. |
FDA Determined Cause 2 | Process design |
| Action | BOMImed sent a "Medical Device Safety Alert & Correction Action" letter by Fax and Mail on 11/25/2010 to the consignee. The product issue was described and recommended actions to mitigate risk were provided. Contact number is 1-800-667-6276 ext. 234. |
| Quantity in Commerce | 30 units |
| Distribution | US Distribution to the state of California. |
| Total Product Life Cycle | TPLC Device Report |
|
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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