| Class 2 Device Recall Medtronic | |
Date Initiated by Firm | December 02, 2022 |
Date Posted | February 25, 2023 |
Recall Status1 |
Open3, Classified |
Recall Number | Z-1176-2023 |
Recall Event ID |
91324 |
510(K)Number | K981128 |
Product Classification |
Suture, nonabsorbable, silk - Product Code GAP
|
Product | Sofsilk Coated Braided Silk Suture Product Description
CS-211 SOFSILK* 4-0 BLK 45CM CVF21 X36 CS211
CS-490 SOFSILK* 2-0 BLK 75CM GS11 X36 CS490
CS-562 SOFSILK* 2-0 BLK 75CM GS23 X36 CS562
GS-823 SOFSILK* 2-0 BLK 75CM V30 X36 GS823
GS-835 SOFSILK* 1 BLK 75CM V20 X36 GS835
S-1172 SOFSILK* 6-0 BLK 45CM C1 X36 S1172
S-1173 SOFSILK* 5-0 BLK 45CM C1 X36 S1173
S-1174 SOFSILK* 4-0 BLK 45CM C1 X36 S1174
S-1750K SOFSILK* 6-0 BLK 45CM HE1 DAX12 S1750K
S-176 SOFSILK* 0 BLK 12X45CM PCT X24 S176
S-176 SOFSILK* 0 BLK 12X45CM PCT X24 S176
S-1768K SOFSILK* 7-0 BLK 45CM HE6 DAX12 S1768K
S-182 SOFSILK* 5-0 BLK 12X45CM PCT X36 S182
S-183 SOFSILK* 4-0 BLK 12X45CM PCT X36 S183
S-184 SOFSILK* 3-0 BLK 12X45CM PCT X36 S184
S-185 SOFSILK* 2-0 BLK 12X45CM PCT X36 S185
S-187 SOFSILK* 1 BLK 6X45CM PCT X36 S187
S-206 SOFSILK* 2 BLK 100CM STDLTH X36 S206
S-243 SOFSILK* 4-0 BLK 12X60CM PCT X36 S243
S-244 SOFSILK* 3-0 BLK 12X60CM PCT X36 S244
S-245 SOFSILK* 2-0 BLK 12X60CM PCT X36 S245
S-246 SOFSILK* 0 BLK 6X60CM PCT X36 S246
S-2782K SOFSILK* 4-0 WHI 45CM SS24 DA S2782K
S-303 SOFSILK* 4-0 BLK 12X75CM PCT X36 S303
S-304 SOFSILK* 3-0 BLK 12X75CM PCT X36 S304
S-305 SOFSILK* 2-0 BLK 12X75CM PCT X36 S305
S-316 SOFSILK* 0 BLK 12X75CM PCT X24 S316
S-317 SOFSILK* 1 BLK 12X75CM PCT X24 S317
S-318 SOFSILK* 2 BLK 12X75CM PCT X24 S318
S-346 SOFSILK* 0 BLK 12X60CM PCT X24 S346
S-605 SOFSILK* 2-0 BLK 2X150CM PCT X36 S605
S-607 SOFSILK* 1 BLK 2X150CM PCT X36 S607
S-608 SOFSILK* 2 BLK 2X150CM PCT X36 S608
SS-523 SOFSILK* 2-0 BLK 75CM SC1 X36 SS523
SS-525 SOFSILK* 1 BLK 75CM SC1 X36 SS525
SS-5641 SOFSILK* 4-0 BLK 45CM P13 X36 SS5641
SS-5641G SOFSILK* 4-0 BLK 45CM P13 X12 SS5641G
SS-5678 SOFSILK* 5-0 BLK 45CM P11 X36 SS5678
SS-5684 SOFSILK* 3-0 BLK 45CM P14 X36 SS5684
SS-623 SOFSILK* 2-0 BLK 75CM SC2 X36 SS623
SS-645 SOFSILK* 4-0 BLK 75CM C12 X36 SS645
SS-653 SOFSILK* 4-0 BLK 75CM C13 X36 SS653
SS-673 SOFSILK* 5-0 BLK 75CM C12 X36 SS673
SS-683G SOFSILK* 4-0 BLK 45CM C13 X12 SS683G
SS-685G SOFSILK* 2-0 BLK 45CM C15 X12 SS685G
SS-686 SOFSILK* 4-0 BLK 45CM C12 X12 SS686
SS-689 SOFSILK* 1 BLK 75CM C16 X36 SS689
SS-745 SOFSILK* 3-0 BLK 75CM C12 X36 SS745
SS-786 SOFSILK* 0 BLK 75CM C14 X36 SS786
SS-787 SOFSILK* 1 BLK 75CM C14 X36 SS787
VS-533 SOFSILK* 2-0 BLK 90CM V20 DAX36 VS533
VS-845 SOFSILK* 1 BLK 75CM V26 X36 VS845
VS-870 SOFSILK* 5-0 BLK 75CM CV23 X36 VS870
VS-871 SOFSILK* 4-0 BLK 75CM CV23 X36 VS871
SOFSILK 4-0 30 BK CV-23 VS871-2 VS8712
VS-872 SOFSILK* 3-0 BLK 75CM CV23 X36 VS872
SOFSILK 3-0 30 BK CV-23 VS872-2 VS8722
VS-882 SOFSILK* 3-0 BLK 75CM CV15 X36 VS882
SOFSILK 5-0 30 BK CV-11 VS890-2 VS8902
XX-5278 SOFSILK* 3-0 BLK 150CM PCT X36 XX5278
XX-5280 SOFSILK* 0 BLK 150CM PCT X36 XX5280
XX-5281 SOFSILK* 1 BLK 150CM PCT X36 XX5281
XX-5284 SOFSILK* 4 BLK 150CM PCT X36 XX5284 |
Code Information |
GTIN:
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Model Number Lot #
CS211 D1L1576Y
D2B0747Y
CS490 D2C2519Y
CS562 D1G1928Y
GS823 D1K1923Y
D2D1396Y
GS835 D1E1757Y
S1172 D2C2304Y
S1173 D2C2305Y
D2E1385Y
S1174 D1M1794FY
D1M2954FY
D1M2984FY
S1750K D2E2348Y
S176 D2B1886Y
S176 D2C1977Y
S1768K D1M1759Y
D2B2217Y
S182 D1L1613Y
D2B0177Y
S183 D1M1421Y
D2E1280Y
S184 D1L3136Y
D1M2895Y
D2D0954Y
D2D0964Y
D2D0967Y
D2D0972Y
S185 D2B2785Y
D2B2877Y
D2B2878Y
D2C1421Y
D2D0957Y
D2D0968Y
D2D0971Y
D2D0984Y
D2D0985Y
D2E2680Y
D2E2767Y
D2E2769Y
S187 D2A1585Y
S206 D1L2658Y
D1M2896Y
D2A1586Y
S243 D1M1020Y
D2D2348Y
S244 D1M1590Y
S245 D2A0559Y
D2C2036Y
D2C2162Y
D2D1871Y
S246 D2E1375Y
S2782K D2F0062Y
S303 D1M1424Y
D2C1472Y
D2D1872Y
D2D2120Y
D2E1496Y
S304 D2B0173Y
D2C2163Y
D2C2805Y
D2D1991Y
D2E1484Y
S305 D1L3282Y
D1L3459Y
D2C1280Y
D2C1281Y
D2C1479Y
D2D0959Y
D2E0907Y
D2E2768Y
D2E2772Y
S316 D1L3311Y
D1M0530Y
D2A0555Y
D2A0557Y
D2A0558Y
D2A0866Y
D2C2806Y
D2D2434Y
D2D2436Y
S317 D2D2087Y
D2E0587Y
S318 D1M0153Y
D2A1677Y
S346 D2A0867Y
D2B1884Y
S605 D1L2686Y
D2B2244Y
S607 D1M2899Y
S608 D1L1617Y
D1L1619Y
D1L1622Y
D1M0173Y
D1M0635Y
D1M0655Y
D2E1210Y
SS523 D2C1971Y
SS525 D1G1346Y
SS5641 D2B2181FY
SS5641G D1D2533FY
SS5678 D1L2430FY
SS5684 D2B1970FY
SS623 D1G0960Y
D2A1069Y
SS645 D1K2457FY
D1L3151FY
D1M2526FY
D1M2531FY
SS653 D1E2737FY
SS673 D1L0164FY
SS683G D1L0794FY
SS685G D2A0503FY
SS686 D1E0201FY
SS689 D2C0024FY
SS745 D1M2971FY
SS786 D1E1220FY
SS787 D1L0032FY
VS533 D1M0598Y
VS845 D2B1779Y
VS870 D1M2873Y
VS871 D1L0602Y
VS8712 D2C3153Y
VS872 D1M1837Y
D2C2945Y
VS8722 D1D3187Y
D1M1292Y
VS882 D1G1139Y
VS8902 D2B0364Y
XX5278 D2B0174Y
XX5280 D2E1482Y
XX5281 D2B0175Y
XX5284 D1L2691Y
|
Recalling Firm/ Manufacturer |
Covidien, LP 60 Middletown Ave North Haven CT 06473-3908
|
For Additional Information Contact | Medtronic Customer Service 800-962-9888 |
Manufacturer Reason for Recall | Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact |
FDA Determined Cause 2 | Packaging process control |
Action | Medtronic issued an "URGENT: MEDICAL DEVICE RECALL" letter to US consignees on 01-Dec-2022 via UPS 2-day delivery. OUS countries, notifications are handled via a regionally approved method.
Letter states reason for recall, health risk and actions to take:
Actions: " Identify and quarantine all unused and non-expired affected non-absorbable sutures.
" Please note the affected product may be located within Custom Suture Packs. Please reference Custom Suture Packs to identify affected product.
" Please complete the enclosed Customer Confirmation Form (even if your account no longer has affected product on hand) and email to rs.gmbfcamitg@medtronic.com.>
" Return all unused and non-expired affected product in your inventory to Medtronic as indicated in the Shipping and Return Instructions below.
" Pass on this notice to all those who need to be aware within your organization or to any organization where the potentially affected product has been transferred or distributed.
Shipping and Return Instructions:
" Product purchased directly from Medtronic please contact rs.covidienfeedbackcustomerservice@medtronic.com for Return Good Authorization (RGA). Your local Medtronic Representative can assist you as necessary in initiating the return of this product.
" Credit or Replacement for the returned affected product will be issued based on the RGA number.
" Return all unused and non-expired affected product(s) in your inventory to:
Medtronic, Attn: Field Returns Dept.
195 McDermott Road, North Haven, CT 06473 USA.
" If purchased from a distributor, contact your distributor directly to arrange for the return of the product back to your distributor.
If you have any questions regarding this communication, please contact your Medtronic Representative or Customer Service at 800-962-9888. |
Quantity in Commerce | 271800 units |
Distribution | US Nationwide Distribution and OUS Foreign distribution to countries of:
Albania
Argentina
Armenia
Australia
Austria
Azerbaijan
Belarus
Belgium
Bosnia And Herzegovina
Brazil
Bulgaria
Cambodia
Cameroon
Canada
Canary Islands
Chile
China
Colombia
Croatia
Czech Republic
Denmark
Egypt
Finland
France
Georgia
Germany
Ghana
Greece
Hong Kong
Hungary
India
Indonesia
Iran
Iraq
Ireland
Israel
Italy
JAPAN
Jordan
Kazakhstan
Kenya
Korea, Republic Of
Kosovo
Kuwait
Latvia
Lebanon
Lithuania
Macao
Malaysia
Malta
Mauritius
Mexico
Moldova, Republic Of
Morocco
Myanmar
Namibia
Netherlands
New Zealand
North Macedonia
Norway
Pakistan
Panama
Paraguay
Philippines
Poland
Portugal
Reunion
Romania
Russian Federation
Saudi Arabia
Serbia
Singapore
Slovakia
Slovenia
South Africa
Spain
Sweden
Switzerland
Syrian Arab Republic
Taiwan
Thailand
Tunisia
Turkey
Uganda
Ukraine
United Arab Emirates
United Kingdom
Uruguay
Uzbekistan
Viet Nam
Zimbabwe
|
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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510(K) Database | 510(K)s with Product Code = GAP
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