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Groshong 7741800Recalls & reported problems

Bard Access Systems, Inc. · Groshong CV Catheter Repair Kit for Use with Groshong 8F Single-Lumen CV Catheter · Class 2

All models of Groshong (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Jan 4, 2023Open, Classified

    Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable).

    Z-1051-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices

All Catheter,intravascular,therapeutic,long-term greater than 30 days devices →

Sources and updates

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