Z-2707-2024Class II
Medline medical procedure kits labeled as follows: a) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, 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) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, REF DYNJ905002B; c) SUCTION MEDI VAC, REF DYKM2033 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-2707-2024
- Classification
- Class II
- Status
- Open, Classified
- Initiated
- Posted
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Medline medical procedure kits labeled as follows: a) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, REF DYNJ905002B; c) SUCTION MEDI VAC, REF DYKM2033
- Product code
- FTN Plastic Surgery And Accessories Kit
- 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
- 3539 units
- Distribution
- Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
- Product codes and lots
- a) REF DYNJ905004C, UDI/DI 40195327316939 (case), 10195327316938 (unit), Lot Numbers: 23CBG213, 23EBI690, 23FBT057, 23GBB635, 23IBA478, 23JBB064; b) REF DYNJ905002B, UDI/DI 40195327316861 (case), 10195327316860 (unit), Lot Numbers: 23ABK521, 23BBG561, 23CBU161, 23EBE334; c) REF DYKM2033, UDI/DI 40193489849241 (case), 10193489849240 (unit), Lot Numbers: 22FMF595, 22HMB247, 22HMD137, 22LMD691, 22LMH566, 23BMG473, 23DMI525, 23FMG464, 23GMH062, 23IMH701, 23KMA183
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.