PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224). Lot Numbers: REDT4257 REDV3617 REDY1815 REDY2789 REDZ0385 REEN2192 REEN2782 REDW2682 REDX1471 REDX3857 REDY0765 REDY1593 REDY2943 REDZ0676 REDZ1903 REDZ3077 REEN1222 REEN3292 REEP0666 REEP4137 REER0612 REDW1021 REDX1360 REDX4728 REDY1816 REDY2935 REDY3765 REDZ1825 REDZ3146 REEN1935 REEP0773 REEP3544 REEP4066 REER0579 REER1103 REDV2172 REDV3683 REDW0467 REDW0521 REDW1023 REDW1157 REDX1361 REDX1490 REDY0815 REDY1594 REDY2790 REDY3544 REDZ0110 REDZ0386 REDZ0677 REDZ1904 REDZ3078 REEN1072 REEN2186 REEN3075 REEN3310 REEP0663 REEP1401 REEP4138 REEQ0611 REEQ1246 REEQ2436 REEQ3589 REER0576 REER1046 REER2161 Additional lot added 10/16/20: REEU0314
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Becton Dickinson & Company
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)
Product Codes/Lot Numbers:
Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224). Lot Numbers: REDT4257 REDV3617 REDY1815 REDY2789 REDZ0385 REEN2192 REEN2782 REDW2682 REDX1471 REDX3857 REDY0765 REDY1593 REDY2943 REDZ0676 REDZ1903 REDZ3077 REEN1222 REEN3292 REEP0666 REEP4137 REER0612 REDW1021 REDX1360 REDX4728 REDY1816 REDY2935 REDY3765 REDZ1825 REDZ3146 REEN1935 REEP0773 REEP3544 REEP4066 REER0579 REER1103 REDV2172 REDV3683 REDW0467 REDW0521 REDW1023 REDW1157 REDX1361 REDX1490 REDY0815 REDY1594 REDY2790 REDY3544 REDZ0110 REDZ0386 REDZ0677 REDZ1904 REDZ3078 REEN1072 REEN2186 REEN3075 REEN3310 REEP0663 REEP1401 REEP4138 REEQ0611 REEQ1246 REEQ2436 REEQ3589 REER0576 REER1046 REER2161 Additional lot added 10/16/20: REEU0314
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2660-2020
Related Recalls
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Becton Dickinson & Company
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
Becton Dickinson & Company
An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush Syringes with this stopper causes an increase in injection force, which has the potential to trigger alarms if used with a syringe pump.
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).