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FDA Medical Device Recalls (openFDA)

Amendia, Inc: Zeus-P Lumbar Interbody Device

Recall number
Z-0827-2017
Recalling firm
Amendia, Inc
Product
Zeus-P Lumbar Interbody Device
Status
Terminated
Initiated
2016-11-22
Posted
2016-12-20
Terminated
2017-06-05
Reason
Labeling error where three boxes in inventory had conflicting patient and primary labels. Evaluation indicated that the primary label and patient label did not match. The primary label matched the label on the inner pouch, but the patient label was incorrect.
Root cause
Error in labeling
Action
Amendia Inc. sent an Urgent - Medical Device Recall letter dated November 22, 2016, to all affected customers. The letter requested that they examine inventory and quarantine the product. The letter also requested that they contact Amendia to confirm receipt of the letter and to obtain a Return Material Authorization for any product on hand. For further questions please call (404) 610-7215.
Quantity
25 units
Distribution
US Distribution to the states of : GA. MI, OK, SC, TX, VA
Lot, serial or model codes
Part Number 1-110926B - Lot Number 128945 and Part Number 1-120922B - Lot Number 128946
510(k) numbers
["K151322"]
PMA numbers
not on file
Product code
MAX
Firm FEI
3007970248
Firm city
Marietta
Firm state
GA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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