Instructions for Use for the blue endo MOREsolution Electromechanical… — Class II medical device recall Z-2145-2014
Terminated recall by Market-Tiers Inc, reported 2014-12-03, distributed nationwide. Some pages of the Instructions for Use were omitted, including pages regarding the Indications for Use, Warnin
| Recall number | Z-2145-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Market-Tiers Inc, Lenexa, KS, United States |
| Recall initiated | 2014-07-16 |
| Classified | 2014-11-21 |
| Reported by FDA | 2014-12-03 |
| Terminated | 2015-05-11 |
| Distributed | Nationwide (US) |
| Quantity | 100 units |
| Serial numbers | 4861300-002, 6283800-002, 6283800-004, 6283800-008, 6283800-010, 6283800-011, 6283800-013, 6283800-014, 6283800-016, 6283800-017, 6283800-019, 6283800-020, 6283800-021, 6283800-022, 6283800-023, 6283800-024, 6283800-026, 6283800-027, 6283800-029, 6283800-030, 6283800-031, 6283800-034, 6283800-037, 6283800-038, 6283800-039 and 75 more |
| Model numbers | 55-000011 |
Product
Instructions for Use for the blue endo MOREsolution Electromechanical Laparoscopic Morcellator System, Model 55-000011, consisting of the control unit, hand-grip, flexible shaft, trocars/obturators, sleeves, valves, and blades.
Reason for recall
Some pages of the Instructions for Use were omitted, including pages regarding the Indications for Use, Warning, and Contraindications.
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-2145-2014. 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.