CrossCHECK Non-Locking Screw in the following sizes: 3 — Class II medical device recall Z-2542-2015
Terminated recall by Wright Medical Technology, Inc., reported 2015-09-09, distributed nationwide. These screws have a potential of passing through the plate in the case when torque is applied in excessive amo
| Recall number | Z-2542-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology, Inc., Memphis, TN, United States |
| Recall initiated | 2015-07-21 |
| Classified | 2015-09-01 |
| Reported by FDA | 2015-09-09 |
| Terminated | 2018-08-01 |
| Distributed | Nationwide (US) |
| Quantity | 5,687 units |
| Reason classes | device malfunction |
| Lot numbers | 0114, 10157-01, 1213, 34995, 34995-1, 34995-10, 34995-11, 34995-12, 34995-13, 34995-14, 34995-15, 34995-16, 34995-17, 34995-18, 34995-19, 34995-2, 34995-20, 34995-21, 34995-22, 34995-22-1, 34995-23, 34995-24, 34995-24-1, 34995-25, 34995-26, 34995-26-1, 34995-27, 34995-28, 34995-28-1, 34995-29, 34995-3, 34995-30, 34995-30-1, 34995-31, 34995-32, 34995-32-1, 34995-33, 34995-34, 34995-34-1, 34995-4 and 56 more |
| Model numbers | CCP-N3008, CCP-N3010, CCP-N3012, CCP-N3014, CCP-N3014L, CCP-N3016, CCP-N3018, CCP-N3020, CCP-N3022, CCP-N3024, CCP-N3026, CCP-N3028, CCP-N3030, CCP-N3032, CCP-N3034, CCP-N3036, CCP-N3038, CCP-N3040, CCP-N3508, CCP-N3510, CCP-N3512, CCP-N3514, CCP-N3516, CCP-N3518, CCP-N3520 and 10 more |
Product
CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm, REF CCP-N3008; 3.0 x 10 mm, REF CCP-N3010; 3.0 x 12 mm, REF CCP-N3012; 3.0 x 14 mm, REF CCP-N3014l; 3.0 x 16 mm, REF CCP-N3016; 3.0 x 18 mm, REF CCP-N3018; 3.0 x 20 mm, REF CCP-N3020; 3.0 x 22 mm, REF CCP-N3022; 3.0 x 24 mm, REF CCP-N3024; 3.0 x 26 mm, REF CCP-N3026; 3.0 x 28 mm, REF CCP-N3028; 3.0 x 30 mm, REF CCP-N3030; 3.0 x 32 mm, REF CCP-N3032; 3.0 x 34 mm, REF CCP-N3034; 3.0 x 36 mm, REF CCP-N3036; 3.0 x 38 mm, REF CCP-N3038; 3.0 x 40 mm, REF CCP-N3040; 3.5 x 8 mm, REF CCP-N3508; 3.5 x 10 mm, REF CCP-N3510; 3.5 x 12 mm, REF CCP-N3512; 3.5 14 mm, REF CCP-N3514; 3.5 x 16 mm, REF CCP-N3516; 3.5 x 18 mm, REF CCP-N3518; 3.5 x 20 mm, REF CCP-N3520; 3.5 x 22 mm, REF CCP-N3522; 3.5 x 24 mm, REF CCP-N3524; 3.5 x 26 mm, REF CCP-N3526; 3.5 x 28 mm, REF CCP-N3528; 3.5 x 30 mm, REF CCP-N3530; 3.5 x 32 mm, REF CCP-N3532; 3.5 x 34 mm, REF CCP-N3534; 3.5 x 36 mm, REF CCP-N3536; 3.5 x 38 mm, REF CCP-N3538; 3.5 x 40 mm, REF CCP-N3540. The CROSSCHECK Plating System is indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones in the hand, feet wrist and ankles, fingers and toes. The system may be used in both pediatric and adult patients. The device is intended for single use.
Reason for recall
These screws have a potential of passing through the plate in the case when torque is applied in excessive amounts, which may result in intraoperative malfunction.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2542-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.