FDA Medical Device Recalls (openFDA)
Nurse Assist, Inc: Case Label: REORDER NO. 6121 STERILE WELCON BRAND 2-Piece 60cc BULB SYRINGE With Sterile Saline 20 ea/Box nurse assist incorporated 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com Tray Label: REORDER NO. 6121 STERILE UNLESS OPENED OR DAMAGED nurse assist incorporated A6010, R1 WELCON BRAND SINGLE USE Bulb Irrigation Tray With 100 mL Sterile Saline 0.9% 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com CONTENTS: 1200 mL Graduated Drain Tray 100 mL Sterile Saline 0.9% 60cc Bulb Syringe Protective Cap Prep Pad Waterproof Underpad Intended use: The trays are irrigation trays for catheters
- Recall number
- Z-2257-2011
- Recalling firm
- Nurse Assist, Inc
- Product
- Case Label: REORDER NO. 6121 STERILE WELCON BRAND 2-Piece 60cc BULB SYRINGE With Sterile Saline 20 ea/Box nurse assist incorporated 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com Tray Label: REORDER NO. 6121 STERILE UNLESS OPENED OR DAMAGED nurse assist incorporated A6010, R1 WELCON BRAND SINGLE USE Bulb Irrigation Tray With 100 mL Sterile Saline 0.9% 800-649-6800 3400 Northern Cross Blvd. Fort Worth, TX 76137 www.nurseassist.com CONTENTS: 1200 mL Graduated Drain Tray 100 mL Sterile Saline 0.9% 60cc Bulb Syringe Protective Cap Prep Pad Waterproof Underpad Intended use: The trays are irrigation trays for catheters
- Status
- Terminated
- Initiated
- 2011-01-20
- Posted
- 2011-05-25
- Terminated
- 2012-10-25
- Reason
- The irrigation procedure trays contain Triad Group Alcohol Prep Pads recalled by Triad Group because they have the potential to be contaminated with an objectionable organism.
- Root cause
- Other
- Action
- The firm, Nurse Assist Incorporated, sent a letter dated January 20, 2011 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to examine their inventory immediately; quarantine the product; identify their customers and notify them at once about the product recall (Nurse Assist will provide bright labels to affix to your affected inventory); provide their customers with labels as well, and complete and return the attached RECALL ACKNOWLEGEMENT form via fax to: 817-231-1500 or mail to: Nurse Assist, Inc., 3400 Northern Cross Blvd., Forth Worth, TX 76137. Only the product and lots identified on the attached list are affected. If you have any questions or to request labels, please call Nurse Assist Customer Service Monday through Friday, from 8:00 am to 5:00 pm Central Time at 1-800-649-6800.
- Quantity
- 80 cases
- Distribution
- Worldwide distribution: USA (nationwide) and countries including: Canada, Dubai and Saudi Arabia.
- Lot, serial or model codes
- Lot Code: 902288 and 1003392
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FCM
- Firm FEI
- 3002695476
- Firm city
- Fort Worth
- Firm state
- TX
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28