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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.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Medline IV Catheter Kits Recalled for Needle Retraction Failure

Agency Publication Date: June 30, 2025
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Summary

Medline Industries, LP. has issued a voluntary recall for 302 convenience kits containing BD Insyte Autoguard Shielded IV Catheters (22 GA x 1.00 IN). The recall was initiated because the needle may retract slowly or fail to retract entirely during insertion into a patient. The affected items include various clinical drawers, emergency trays, and specialty packs used in healthcare settings.

Risk

If the safety needle fails to retract into its protective shield, it creates a risk of accidental needle-stick injuries for healthcare providers. Such injuries could lead to the transmission of bloodborne pathogens or other infections.

What You Should Do

  1. This recall affects Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters (22 GA x 1.00 IN) sold under labels such as CC Drawer, Pedi Emergency Tray, Adult Drawer, IV Start Box, and Retinal Pack.
  2. Identify if you have the affected products by checking the lot numbers (including 24LDA269, 24LDA106, 24LDA823, 24LDB092, 24LDA268, 24LDA260, 24LDA590, and 24LDA980) and reference numbers on the kit labels. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled kits immediately.
  4. Contact Medline Industries or your medical supply distributor to arrange for the return, replacement, or correction of any remaining inventory.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters
Variants: CC DRAWER 4 IV CIRCULATION, CC ADULT DRAWER 2, PEDI EMERGENCY TRAY-BLUE, ADULT DRAWER 4, DRAWER 4 - SUMMIT, DRAWER 3
Model / REF:
ACC010254B
ACC010256
ACC010316A
ACC010389C
ACC010627
ACC010898
Lot Numbers:
24LDA269
24LDA106
24LDA823
24LDB092
24LDA268
24LDA260
UDI:
10193489651683
40193489651684
10884389559529
40884389559520
10889942831746
40889942831747
10193489472493
40193489472494
10195327226589
40195327226580
10198459192074
40198459192075

Recall #: Z-2043-2025; Quantity: 186 units

Product: IV START BOX (containing BD Insyte Autoguard Shielded IV Catheter)
Model / REF:
ACC010665
Lot Numbers:
24LDA590
UDI:
10195327334918
40195327334919

Recall #: Z-2044-2025; Quantity: 36 units

Product: RETINAL PACK-LF (containing BD Insyte Autoguard Shielded IV Catheter)
Model / REF:
DYNJ0151148B
Lot Numbers:
24LDA980
UDI:
10889942050819
40889942050810

Recall #: Z-2045-2025; Quantity: 80 units

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97027
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Hospitals; Surgical Centers; Medical Supply Distributors
Manufactured In: United States
Units Affected: 3 products (186 units; 36 units; 80 units)
Distributed To: Indiana, Kentucky, California, Michigan, Texas, Washington

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.