Date Initiated by Firm | May 20, 2014 |
Date Posted | August 29, 2014 |
Recall Status1 |
Terminated 3 on August 14, 2017 |
Recall Number | Z-2344-2014 |
Recall Event ID |
68536 |
Product Classification |
Accessories, operating-room, table (kit) - Product Code FWZ
|
Product | ARTHROSCOPY PACK - -
(1) MAYO STAND COVER REINFORCED LIF
(3) TOWELS ABSORBENT 15" X 20" LIF
(1) STOCKINETTE IMPERVIOUS 14" X 48" LIF
(1) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK LIF
(1) BLADE SURGICAL # 11 STAINLESS STEEL
(1) NEEDLE HYPODERMIC 21G X 1 ~ LIF
(1) TUR Y SET 81" 2.1M REGULAR CLAM
(1) NEEDLE HYPODERMIC 18G X 1 ~
(1) SHEET ARTHROSCOPY T STD SMS WITH POUCH LIF
(1 0) GAUZE SPONGE 4" X 4" 16PL Y
(1) SHEET DRAPE 70" X 100" LIF
(1) *Pr. SURGEON NEUTRALON GLOVE #8 LATEX
(2) GOWN IMPERVIOUS REINFORCED X-LARGE SMS
(1 0) GAUZE SPONGE 4" X 4" 16PL Y XRD LIF
(1 ) TUBE SUCTION CONNECT. X" X 12' LIF
(1) U-DRAPE 60" X 70" WITH TAPE SPLIT 6" X 21"
(1 ) DURAPREP SURGICAL SOLUTION 26ML LIF
(1 ) NEEDLE SPINAL ANEST. 18G X 3 %" LIF
(2) ELASTIC BANDAGE 6" X 5YRD. LIF
(1) TABLE COVER REINFORCED 50" X 90" LIF
(1) PAD ABDOMINAL 8" X 7.5"
(1) *Pr. SURGEON NEUTRALON GLOVE #8 ~ LATEX
EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents. |
Code Information |
Product code 900-740, 20 lots: 112030744 112041351 112052010 112062505 112072876 112093641 112104101 112114588 112125111 113015457 113025967 113036380 113057877 113088887 113099452 113099576 131110272 131210839 140111248 140211735 |
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 | 20 lots; 1356 units (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 |
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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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