| Date Initiated by Firm |
May 20, 2014 |
| Date Posted |
August 29, 2014 |
| Recall Status1 |
Terminated 3 on August 14, 2017 |
| Recall Number |
Z-2370-2014 |
| Recall Event ID |
68536 |
| Product Classification |
Obstetrical kit - Product Code OKV
|
| Product |
PERl GYN PACK-
(1) DRAPE UTILITY WITH TAPE UF
(2) TOWELS ABSORBENT 15" X 20" UF
(1) TOP DRAPE WITH ADHESIVE STD SMS
(1) CATHETER NELATON ROB. 14FR.
(2) GOWN IMPERVIOUS EXTRA REINFORCED XL
(1) UNDERBUITOCK DRAPE WITH POUCH
(2) LEGGINS WITH 7" CUFF 30" X 42"
(1) TABLE COVER REINFORCED 44" X 78" UF
(1 0) GAUZE SPONGES 4" X 4" 16PL Y XRD LIF
EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents. |
| Code Information |
Product code 900-1061, 43 lots: 110051144 110061480 110071614 110082107 110102421 110112595 110123081 111010014 111020502 111030541 111030814 111040868 111061579 111071751 111082041 111082267 111092342 111102654 111112942 112020305 112051670 112062315 112072764 112083153 112093849 113025926 113026038 113036447 113046995 113047194 113057377 113057824 113068139 113078455 113099265 113099585 131110150 131210675 131211024 140311916 140312431 140412826 140513473 |
Recalling Firm/
Manufacturer |
Customed, Inc
Calle Igualdad Final #7
Fajardo PR 00738
|
| For Additional Information Contact |
Rosemari Melendez
787-622-5151 Ext. 7540
|
Manufacturer Reason
for Recall |
Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
|
FDA Determined
Cause 2 |
Package design/selection |
| Action |
Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit.
Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540 |
| Quantity in Commerce |
43 lots; 3201units (multiple units per lot) |
| Distribution |
Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico. |
| 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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