FDA recall, , Moderate risk
Silastic Foley Catheters
Silastic Foley Catheters have a stain on their surface.
Summary by Recall Canary from the FDA notice
What happened
C.R. Bard Inc of Covington, Georgia, recalled Silastic Foley Catheters Silastic Brand Foley Catheter 30cc and Silastic Brand Foley Catheter 5cc because a stain was present on the surface of the affected catheters. The recall began April 23, 2026, and was added to the FDA's Enforcement Report on May 21, 2026. The products were distributed in the U.S. across many states and in Canada.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI and lot code are listed under that product.
Incomplete list: 40 of 52 lot codes shown.
A UDI-DI is the device identifier printed with the barcode on the device label.
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624
- UDI-DI
- 00801741019982
- 10801741019989
- 00801741019999
- 10801741019996
- 00801741020001
- 10801741020008
- 00801741020018
- 10801741020015
- 00801741020025
- 10801741020022
- 00801741020056
- 10801741020053
- 00801741020063
- 10801741020060
- 00801741020070
- 10801741020077
- 00801741020087
- 10801741020084
- 00801741020094
- 10801741020091
- 00801741020100
- 10801741020107
- Lot code
- NGKX0444
- 33418
- NGKW2813
- 33420
- NGKQ1015
- 33422
- NGKW3707
- 33424
- NGKW2669
- 5cc
- NGKN4037
- NGKP1420
- NGKQ0040
- NGKQ3901
- NGKS4937
- NGKV3462
- NGKW3897
- 33616
- NGKQ0042
- NGKQ3946
- NGKR3420
- NGKT3281
- NGKU1015
- NGKV0617
- NGKV2275
- NGKV2309
- NGKW3771
- 33618
- NGKQ3370
- NGKS3753
- NGKT3258
- NGKT3309
- NGKU4129
- NGKV1446
- NGKV2345
- NGKV3478
- NGKV5029
- 33620
- NGKS5060
- NGKT3308
Recall details
- Company began the recall
- Sold in
U.S.: Alaska, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, and Wisconsin O.U.S.: Canada
- Company
- C.R. Bard IncCovington, Georgia
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98716
- Recall number
- Z-2226-2026
All recalls from C.R. Bard Inc
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
