FDA Device recall Z-2661-2020
PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit
- FDA Device
- Class II
- terminated
- Published 2020-07-29
On 2020-07-29 the FDA classified a Class II recall of PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit by Becton Dickinson And, citing potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2661-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-19 |
| Published | 2020-07-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | n/a |
Product
PowerLoc MAX Power-Injectable Infusion Set myPICK Port Access Kit; Catalog Numbers CPA00001 (UDI 00801741098345), CPA00002 (UDI 00801741098352), CPA00028 (UDI 00801741129728), CPA00032 (UDI 00801741137501), CPA00033 (UDI 00801741137501), CPA00036 (UDI 00801741138911), CPA00051 (UDI 00801741175718), CPA00055 UDI 00801741182181), CPA00056 (UDI 00801741182907)
Reason
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
Identifiers
| code_info | Catalog Numbers CPA00001 (UDI 00801741098345), CPA00002 (UDI 00801741098352), CPA00028 (UDI 00801741129728), CPA00032 (…Catalog Numbers CPA00001 (UDI 00801741098345), CPA00002 (UDI 00801741098352), CPA00028 (UDI 00801741129728), CPA00032 (UDI 00801741137501), CPA00033 (UDI 00801741137501), CPA00036 (UDI 00801741138911), CPA00051 (UDI 00801741175718), CPA00055 UDI 00801741182181), CPA00056 (UDI 00801741182907). Lot Numbers: REEN0212 REEP2685 REEP3660 REEQ3563 REER1968 REDZ0705 REEP3313 REEP3547 REER0577 REEN0214 REEQ3569 REDY3552 REEN1934 REEP3280 REEP3552 REER1115 REEN0218 REEP3659 REEP1436 REER0298 REER1335 REDY0992 REEN0278 REEP1437 REEQ0232 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2661-2020%22
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