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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Compress, Mini Compress; Item Nos. 178350
178351
178352
178353
178354
178355
178356
178357
1...
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2
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11/22/2019
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Zimmer Biomet, Inc.
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Compress Device Short Anchor Plug, 28 MM-For Correction of revision of unsuccessful osteotomy, arthr...
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2
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11/21/2023
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Biomet, Inc.
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Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthr...
|
2
|
11/21/2023
|
Biomet, Inc.
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Compress Device Short Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthr...
|
2
|
11/21/2023
|
Biomet, Inc.
|
Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthr...
|
2
|
11/21/2023
|
Biomet, Inc.
|
Compress Device Short Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthr...
|
2
|
11/21/2023
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Biomet, Inc.
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Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthr...
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2
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11/21/2023
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Biomet, Inc.
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Compress Device Short Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthr...
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2
|
11/21/2023
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Biomet, Inc.
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Compress Device Short Anchor Plug, 16 MM- Correction of revision of unsuccessful osteotomy, arthrode...
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2
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11/21/2023
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Biomet, Inc.
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Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthr...
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2
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11/21/2023
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Biomet, Inc.
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