Synthes Sciatic Nerve Retractor and Sciatic Nerve recall
Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific…
Why was Synthes Sciatic Nerve Retractor and Sciatic Nerve recalled?
Potential for micropores to form, allowing fluid to enter the hollow handle.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part Numbers 03.100.013 03.100.014 with lot numbers: 5001180 5001181 5043720 5043721 5043722 5043723 5056224 5056410 5056411 5101097 5106064 5109323 5162016 5207917 5252353 5252354 5303914 5303916 5626912 904732 / A7OA43 908057 / A7PA10 909551 / A7PA20 910819 / A7PA30 T100870 T104992 T108114 T114599 T938508 T939338 T939640 T942069 T945414 T946497 T949375 T954443 T958062 T963371 T968151 T968381 T972086 T974174 T974550 T977901 T980418 T980555 T983069 T984285 T987813 T993091 T996572 T999967 5001182 5001183 5042920 5042921 5042922 5042923 5056851 5087081 5087082 5109324 5109325 5109326 5109327 5162012 5207918 5252394 5256421 5256479 5256480 5305758 5305759 5305760 5877095 6040220 6040225 6040226 6056133 6056134 903786 / A7OA37 904731 / A7OA43 908058 / A7PA10 909552 / A7PA20 910911 / A7PA31 T100871 T104993 T108115 T114598 T932954 T935264 T939339 T945413 T946498 T947785 T954444 T958061 T963372 T968152 T974175 T977904 T980511 T983070 T984228 T987809 T989000 T993092 T996565 T999969
- Product
- Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific…
- Recalling firm
- Synthes (USA) Products LLC
- Quantity
- 1113
- Distribution
- Nationwide and internationally, including Canada
- Recall date
- August 26, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)