Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Reported: May 21, 2025 Initiated: March 31, 2025 #Z-1743-2025
Product Description
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Reason for Recall
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Details
- Recalling Firm
- AVID Medical, Inc.
- Units Affected
- 72 units
- Distribution
- US Nationwide distribution in the states of IL & LA.
- Location
- Toano, VA
Frequently Asked Questions
What product was recalled? ▼
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.. Recalled by AVID Medical, Inc.. Units affected: 72 units.
Why was this product recalled? ▼
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 21, 2025. Severity: Moderate. Recall number: Z-1743-2025.
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