Z-2703-2024Class II
Medline medical procedure kits labeled as follows: a) BASIC NASAL, REF DYNJ909932; b) BRONCH KIT, REF...
MEDLINE INDUSTRIES, LP - Northfield / initiated 2024-03-22 / Open, Classified
MEDLINE INDUSTRIES, LP - Northfield began a recall of 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... on . FDA classified it as Class II and gives the reason as "A slight dimensional variation which has the potential for increased difficulty fitting into outer canister". As of , the recall status on record is Open, Classified.
Recall record
- Recall number
- Z-2703-2024
- Classification
- Class II
- Status
- Open, Classified
- Initiated
- Posted
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- 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
- Product code
- OGR Ear, Nose, And Throat Surgical Tray
- Reason for recall
- A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
- FDA root cause
- Under Investigation by firm
- Action
- Medline Industries issued a Safety Alert to its consignees on 03/22/2024 via email and certified mail. The notice explained the problem with the device and requested that consignees follow the instructions for use. Distributors or those who further transferred the affected product were directed to notify their consignees.
- Quantity in commerce
- 6998 units
- Distribution
- Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
- Product codes and lots
- a) REF DYNJ909932, UDI/DI 40195327511167 (case), 10195327511166 (unit), Lot Numbers: 23JBI290, 23KBI103; b) REF DYKE1007B, UDI/DI 40195327203697 (case), 10195327203696 (unit), Lot Numbers: 22HBF709, 22HBV977, 22LBC080, 22LBH793, 23CBP363, 23DBL601, 23EBT148, 23FBS311, 23GBP583, 23HBY932, 23JBK265,; c) REF DYNJ909935, UDI/DI 40195327511198 (case), 10195327511197 (unit), Lot Numbers: 23JBH869; d) REF DYNJ902624G, UDI/DI 40195327214525 (case), 10195327214524 (unit), Lot Numbers: 22IBA877, 22IBN753, 23DBG397, 23FBN458, 23GBG939, 23HBT691, 23JBQ259, 23KBO185; e) REF DYNJ902377I, UDI/DI 40195327505883 (case), 10195327505882 (unit), Lot Numbers: 23JBI663; f) REF DYNJ65475B, UDI/DI 40195327303519 (case), 10195327303518 (unit), Lot Numbers: 22LBE939, 23ABK037, 23BBI110, 23CBH860, 23DBF474, 23DBS953, 23GBN857, 23JBE718, 23KBL576; g) REF DYNJ65487B, UDI/DI 40195327303663 (case), 10195327303662 (unit), Lot Numbers: 22LBP408, 23ABN443, 23CBM523, 23DBM713, 23IBM894; h) REF DYNJ906898, UDI/DI 40193489281928 (case), 10193489281927 (unit), Lot Numbers: 22HBA414, 22JBR764, 23FBK308, 23GBC593, 23IBF940, 23KBO165, 23KBT057; i) REF DYNJ906897B, UDI/DI 40195327373147 (case), 10195327373146 (unit), Lot Numbers: 23EBE963, 23EBL760, 23FBC942, 23FBC943, 23HBQ553, 23HBS215, 23IBD903, 23KBE192, 23KBI100, 23LBH012; j) REF DYNJ906914, UDI/DI 40193489280174 (case), 10193489280173 (unit), Lot Numbers: 22EBS455, 22EBU139, 22GBK146, 22HBG371, 22JBG419, 22KBI283, 23ABC387, 23CBI473, 23CBO589, 23CBU019, 23EBE957, 23EBV972, 23GBB581, 23IBP952, 23IBV288, 23JBB697, 23LBJ608; k) REF DYNJ909941, UDI/DI 40195327511006 (case), 10195327511005 (unit), Lot Numbers: 23JBH984
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-2694-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2695-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2696-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2697-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2698-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2699-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2700-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2701-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2702-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2703-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2704-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2705-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2706-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2707-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2708-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2709-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2710-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2711-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2712-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2713-2024 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-2714-2024 | Class II | Ongoing | Voluntary: Firm initiated |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.