FDA Device recall Z-0150-2014
Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids
- FDA Device
- Class II
- terminated
- Published 2013-11-13
On 2013-11-13 the FDA classified a Class II recall of Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids by Ethicon Endo Surgery, citing during aging studies, the firm determined that the gastric belts were unable to pass the test requirements established for Force to Lock.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0150-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-30 |
| Published | 2013-11-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ethicon Endo Surgery |
| Distribution | US |
Product
Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids. Product Usage: Intended for use in surgical treatment of morbid obesity
Reason
During aging studies, the firm determined that the gastric belts were unable to pass the test requirements established for Force to Lock.
Identifiers
| code_info | The following product code and lot numbers were affected by this recall: Product Codes: 2200-X Lot Numbers: ZLGBC5, Z…The following product code and lot numbers were affected by this recall: Product Codes: 2200-X Lot Numbers: ZLGBC5, ZLNBCW, ZLNBJC, ZLPBB9, ZMBBBB, ZMCBBC, ZMGBCJ, ZMHBBT, ZMHBCV, ZMLBD0, ZMMBCD, ZMPBBC, ZNCBC6, ZNGBB3, and ZNGBBF. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0150-2014%22
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