ROi Consolidated Service Center (CSC): Medical Device Recall in 2019 - (Recall #: Z-2220-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Regard ¿ custom surgical pack labeled as "LAP - FLOL LADY OF ANGELS" including recalled Stryker part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP and 0620 040 680 Pneumosure High Flow Tubeset with RTP.

Product Classification:

Class II

Date Initiated: March 21, 2019

Date Posted: August 14, 2019

Recall Number: Z-2220-2019

Event ID: 82499

Reason for Recall:

Resource Optimization & Innovation (ROi) has received a recall notice from Stryker regarding tube sets potentially detaching from the cassette, which can lead to leaking gas or a hissing sound.

Status: Ongoing

Product Quantity: 261 packs

Code Information:

Item Number (Lot Number, Expiration Date): 800096004 (044343D, 43590); 800096004 (048023D, 43722); 800096004 (049262D, 43757); 800096004 (052020D , 43856); 800096004 (054482D, 43948); 800096004 (057619D, 44035); 800096005 (059908E , 44080); 800096005 (062938E , 44151); 800096005 (65606E, 44232);

Distribution Pattern:

Distributed to LA and MO

Voluntary or Mandated:

Voluntary: Firm initiated