FDA Device recall Z-0118-2023

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

FDA Device
Class II
ongoing
Published 2022-11-02

On 2022-11-02 the FDA classified a Class II recall of AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR by Zoll Circulation, citing due to increase in Li-Ion Battery failures.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0118-2023
Classification	Class II
Status	ongoing
Initiated	2022-09-22
Published	2022-11-02
Last updated	2026-09-13 11:56 UTC
Company	Zoll Circulation
Distribution	AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TX, UT, VA, VT, WA, WI, WV, WY

Product

AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR

Reason

Due to increase in Li-Ion Battery failures

Identifiers

code_info	Model Number: 100 UDI-DI Codes: (01)00849110 Part Nos. 12742-001 12742-002 12742-003 12742-004 12742-005 12742-006 1274… Model Number: 100 UDI-DI Codes: (01)00849110 Part Nos. 12742-001 12742-002 12742-003 12742-004 12742-005 12742-006 12742-008 12742-009 12742-010 12742-011 12742-012 12742-013 12742-014 12742-007 12742-015 12742-016 12742-017 12742-019 Serial Numbers: U.S. 6530 6532 6539 6541 6542 6543 6549 6550 6553 6554 6555 6556 6557 6559 6563 6564 6565 6566 6572 6573 6575 6576 6577 6578 6580 6581 6582 6583 6586 6588 6589 6590 6591 6595 6597 6598 6599 6602 6605 6606 6608 6609 6611 6612 6613 6614 6617 6619 6620 6621 6622 6623 6626 6627 6628 6630 6632 6635 6636 6638 6639 6641 6642 6644 6645 6647 6650 6652 6653 6654 6655 6656 6658 6659 6660 6661 6662 6663 6665 6667 6668 6669 6670 6671 6672 6674 6677 6679 6681 6682 6683 6684 6685 6688 6690 6691 6692 6693 6694 6695 6696 6697 6698 6699 6700 6701 6702 6704 6705 6706 6707 6708 6709 6710 6711 6712 6713 6714 6715 6716 6717 6718 6719 6720 6721 6722 6724 6725 6726 6727 6728 6729 6730 6732 6734 6735 6736 6737 6738 6739 6740 6742 6744 6745 6746 6747 6749 6750 675

code_info

Model Number: 100 UDI-DI Codes: (01)00849110 Part Nos. 12742-001 12742-002 12742-003 12742-004 12742-005 12742-006 1274…

Model Number: 100 UDI-DI Codes: (01)00849110 Part Nos. 12742-001 12742-002 12742-003 12742-004 12742-005 12742-006 12742-008 12742-009 12742-010 12742-011 12742-012 12742-013 12742-014 12742-007 12742-015 12742-016 12742-017 12742-019 Serial Numbers: U.S. 6530 6532 6539 6541 6542 6543 6549 6550 6553 6554 6555 6556 6557 6559 6563 6564 6565 6566 6572 6573 6575 6576 6577 6578 6580 6581 6582 6583 6586 6588 6589 6590 6591 6595 6597 6598 6599 6602 6605 6606 6608 6609 6611 6612 6613 6614 6617 6619 6620 6621 6622 6623 6626 6627 6628 6630 6632 6635 6636 6638 6639 6641 6642 6644 6645 6647 6650 6652 6653 6654 6655 6656 6658 6659 6660 6661 6662 6663 6665 6667 6668 6669 6670 6671 6672 6674 6677 6679 6681 6682 6683 6684 6685 6688 6690 6691 6692 6693 6694 6695 6696 6697 6698 6699 6700 6701 6702 6704 6705 6706 6707 6708 6709 6710 6711 6712 6713 6714 6715 6716 6717 6718 6719 6720 6721 6722 6724 6725 6726 6727 6728 6729 6730 6732 6734 6735 6736 6737 6738 6739 6740 6742 6744 6745 6746 6747 6749 6750 675

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0118-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.