Reported Jun 11, 2025 · Ongoing

Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.

Mozarc Medical US LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mozarc Medical US LLC · 15 Hampshire St · Mansfield, MA · 02048-1113

Is this the product you have?

  • Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Lot codes and dates
    • Model No. 8888128450P
    • 8888123404P
    • 8888123410P
    • 8888128454P
    • 8888128460P
    • 8888133500P
    • 8888133504P
    • 8888133510P
    • 8888123400P
    • 8888119360P
    • 8888119370P
    • 8888119364P
  • UDI

    162 of 162 codes

    • A8845211578301
    • A8845211577701
    • A8845211578101
    • A8845211578401
    • A8845211578801
    • A8845211579001
    • A8845211579101
    • 20884521157955
    • A8845211577601
    • A8845211576901
    • A8845211577401
    • A8845211577001
    • UPN 20884521157832
    • 20884521157771
    • 20884521157818
    • 20884521157849
    • 20884521157887
    • 20884521157900
    • 20884521157917
    • 10884521157767
    • 20884521157764
    • 20884521157696
    • 20884521157740
    • 20884521157702
    • Lot/Serial No. 240450106
    • 240640172
    • 240640173
    • 240640180
    • 240640210
    • 240660013
    • 240780122
    • 240790012
    • 240850175
    • 240850176
    • 241170007
    • 241270012
    • 241340007
    • 241340289
    • 241410006
    • 241550024
    • 241620025
    • 241690028
    • 241800007
    • 241900044
    • 241970039
    • 242110216
    • 242110217
    • 242110218
    • 242180246
    • 242180247
    • 242180248
    • 242180253
    • 242180254
    • 2119700109
    • 2130800058
    • 2130800068
    • 2130800101
    • 2133500082
    • 2133600117
    • 2133700190
Amount recalled
95,938 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential breach of sterile barrier packaging.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.