Medline medical procedure kits labeled as follows: a) BASIC NASAL — Class II medical device recall Z-2703-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-08-28, distributed nationwide. A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
| Recall number | Z-2703-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-03-22 |
| Classified | 2024-08-22 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO, MX, OM, PA, QA, SG, SV |
| Quantity | 6,998 units |
| UPC / GTIN / UDI-DI | 10193489280173, 10193489281927, 10195327203696, 10195327214524, 10195327303518, 10195327303662, 10195327373146, 10195327505882, 10195327511005, 10195327511166, 10195327511197, 40193489280174, 40193489281928, 40195327203697, 40195327214525, 40195327303519, 40195327303663, 40195327373147, 40195327505883, 40195327511006, 40195327511167, 40195327511198 |
| Lot numbers | 22EBS455, 22EBU139, 22GBK146, 22HBA414, 22HBF709, 22HBG371, 22HBV977, 22IBA877, 22IBN753, 22JBG419, 22JBR764, 22KBI283, 22LBC080, 22LBE939, 22LBH793, 22LBP408, 23ABC387, 23ABK037, 23ABN443, 23BBI110, 23CBH860, 23CBI473, 23CBM523, 23CBO589, 23CBP363, 23CBU019, 23DBF474, 23DBG397, 23DBL601, 23DBM713, 23DBS953, 23EBE957, 23EBE963, 23EBL760, 23EBT148, 23EBV972, 23FBC942, 23FBC943, 23FBK308, 23FBN458 and 32 more |
| Model numbers | DYKE1007B, DYNJ65475B, DYNJ65487B, DYNJ902377I, DYNJ902624G, DYNJ906897B, DYNJ906898, DYNJ906914, DYNJ909932, DYNJ909935, DYNJ909941 |
Product
Medline medical procedure kits labeled as follows: a) BASIC NASAL, REF DYNJ909932; b) BRONCH KIT, REF DYKE1007B; c) ENT, REF DYNJ909935; d) NASAL SINUS-LF, REF DYNJ902624G; e) ORAL, REF DYNJ902377I; f) PACK,BRONCHOSCOPY, REF DYNJ65475B; g) PACK,HEAD AND NECK, REF DYNJ65487B; h) PACK,SINUS, REF DYNJ906898; i) PACK,T & A, REF DYNJ906897B; j) PACK,T & A ASC, REF DYNJ906914; k) T AND A, REF DYNJ909941
Reason for recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
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-2703-2024. 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.