Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

MEDLINE INDUSTRIES, LP - Northfield: Centurion Procedure Kits Recalled for Defective Syringes

Agency Publication Date: August 28, 2024
Share:
Sign in to monitor this recall

Summary

Medline Industries is recalling several types of Centurion medical convenience and procedure kits, including biopsy, arterial line, chest tube, and umbilical vessel trays. These kits contain plastic syringes that were part of an FDA Safety Alert issued on March 19, 2024. Quality issues including leaks, breakage, and other performance failures have been identified with these syringes, which can disrupt critical medical procedures.

Risk

The plastic syringes in these kits may leak or break during use, which can lead to improper medication delivery, procedure delays, or potential exposure to contaminants, posing a risk of injury to patients during sensitive medical interventions.

What You Should Do

  1. Identify if you have any affected Centurion procedure kits by checking the 'Pack Number' and 'Lot Number' on the external kit packaging. Affected pack numbers include common medical kits like CHT560 (Chest Tube), SUT20455 (Biopsy Skin), and PT220 (Arthrogram/LP/Myelogram).
  2. Verify your specific lot number against the extensive list of recalled codes, such as 2022040190, 2021092290, 2023121290, and many others listed in the product data.
  3. If an affected kit is found, immediately stop using it and set it aside to ensure it is not used in a medical procedure.
  4. Contact your healthcare provider or Medline Industries directly to report the possession of affected kits and to receive instructions on how to return or dispose of the product.
  5. Healthcare professionals should contact Medline at 1-800-MEDLINE or visit their website for specific details on replacement products or credits for returned inventory.
  6. For additional information or to report a safety issue, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Contact healthcare provider or manufacturer for instructions.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Centurion BIOPSY KIT
Model / REF:
DYNDA1466A
Lot Numbers:
2022040190
2022092690
Product: Centurion BIOPSY SKIN/LACERATION TRAY
Model / REF:
SUT20455
Lot Numbers:
2022040190
2021060190
2022011090
2023012390
2018090690
2019022590
2019042990
2019101690
2019112590
2020040690
2021042190
2021062590
2021081090
2022070590
2023070590
2023100590
2023122990
Product: Centurion CHEST TUBE INSERTION TRAY
Model / REF:
CHT560
Lot Numbers:
2021092290
2018042790
2018050790
2018060490
2018080790
2018091190
2020032490
2020051990
2020062490
2020070190
2020071490
2020121590
2021042690
2021082390
2021091490
2022022490
2022050490
Product: Centurion CUSTOM BIOPSY TRAY
Model / REF:
MNS4815
Lot Numbers:
2022040190
2021100590
2021122890
2023011390
2023012090
2023061590
2022042890
Product: Centurion PERITONSILLAR ABSCESS TRAY
Model / REF:
MNS3560
Lot Numbers:
2021021790
2021092290
2021092890
2022040190
2022071490
2023121290
2021091490
Product: Centurion PRE POST DIALYSIS
Model / REF:
DYNDC3274
Lot Numbers:
2023121290
2023013090
Product: Centurion STEREO PROCEDURE TRAY
Model / REF:
DYNDC2859A
Lot Numbers:
2021092290
2021082390
2021113090
2022101990
2022111890
2023012690
2023083190
2020081790
2023053090
Product: Centurion UMBILICAL VESSEL TRAY
Model / REF:
UVT1100
UVT1100A
Lot Numbers:
2021032280
2021072680
2021092780
2022011080
2022050280
2023011680
2023041780
2023061980
2023101680
2023120480
2024011580
Product: Centurion BREAST BIOPSY PACK
Model / REF:
BT515A
MNS6950A
Lot Numbers:
2018101150
2019022550
2019040350
2020040990
2021062990
2022012090
2022022890
2022072990
2022103190
2023031790
2023032890
2023072590
2024022990

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94585
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Authorized Medical Distributors; Hospitals; Medical Facilities
Manufactured In: United States
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.