FDA Recall Terminated

Jet-Ventilator Catheter for Adults, 14G, STERILE, NO LATEX, REF 30-02-914-1, VBM Medizintechnik GmbH, Einsteinstrasse 1 7212 Sulz a.N. Germany Allows a safe and atraumatic transtracheal access for oxygenation/ventilation with a manual jet ventilator or an automatic high frequency jet ventilator.

Recall: Z-2675-2011 · Initiated May 9, 2011

Recall

Recall Number
Z-2675-2011
Event Number
58807
Firm
VBM Medical Inc.
FEI Number
3003316541
Product Code
BTO
Status
Terminated
Root Cause
Error in labeling
Initiated
May 9, 2011
Posted
June 28, 2011
Terminated
March 14, 2012
Address
524 Herriman Ct, Noblesville, IN, 46060-4363

Description

Jet-Ventilator Catheter for Adults, 14G, STERILE, NO LATEX, REF 30-02-914-1, VBM Medizintechnik GmbH, Einsteinstrasse 1 7212 Sulz a.N. Germany Allows a safe and atraumatic transtracheal access for oxygenation/ventilation with a manual jet ventilator or an automatic high frequency jet ventilator.

Reason

Product labeled with incorrectly as being appropriate for use in adults when the intended population for use of the product is children and infants.

Action

VBM Medical Inc sent an "URGENT FIELD SAFETY NOTICE" dated May 9, 2011, to all affected customers. The letter identified the product, the problem, and the action needed to be taken by the customer. The reference and lot numbers, details of the error, along with the incorrect and correct box label, and instructions to the customers to discard the box with the incorrect label or send the complete product back to VBM Medical Inc. for re-packaging. For any further or detailed questions, please contact VBM Medical Inc. at (317) 776-1800. On 7/12/11 upon receiving the recall classification letter, the firm sent out an additional letter to its direct accounts informing them of the recall's classification and reiterating the instructions listed above.

Distribution

Worldwide Distribution -- USA ( nationwide ) including the country Montreal QC

Quantity

388