Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the he
FDA device recall Z-1679-2017 · posted 2017-03-24 · Terminated
Recall details
- Recalling firm
- Molded Products Inc
- Reason for recall
- A customer relayed a complaint of a leaking dialysis tubing connector.
- Action taken
- On 1/20/2015, the recalling firm requested the firm's customer to return units from the affected lot.
- Root cause
- Process control
- Status
- Terminated
- Product code
- KOC
- Quantity affected
- 400 pieces
- Distribution
- Product was distributed to Ontario, Canada.
- Date initiated
- 2015-01-20
- Date posted
- 2017-03-24
- Date terminated
- 2017-03-30
- Location
- Harlan, IA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MODIFICATION TO MALE TO MALE LUER ADAPTER (K003712) | Molded Products, Inc. | 2001-05-16 |