HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.

Class I - Dangerous
🏥 Medical Devices Recalled: September 14, 2017 C.R. Bard Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Item 50610 Lots #'s: JUBT0404, JUBP0700, JUBR2498, JUBS1289
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
C.R. Bard, Inc.
Reason for Recall:
Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual pouch. MGC3 Product Usage Intermittent catheters are intended for urinary bladder drainage in patients requiring catheterization for management of incontinence, voiding dysfunction, and surgical procedures.

Product Codes/Lot Numbers:

Item 50610 Lots #'s: JUBT0404, JUBP0700, JUBR2498, JUBS1289

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1307-2018

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