FDA recall record

AVID Medical Halyard SUTURE PACK CABG recall — FDA Z-1742-2025

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…

Class IIclassification
Z-1742-2025official record ID
May 21, 2025report date

Recall record at a glance

Official recordZ-1742-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAVID Medical, Inc.
Report dateMay 21, 2025
Recall initiation dateMar 31, 2025
Quantity60 units
LocationToano, VA, United States

Official product description

Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.

Why the product was 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.

Distribution information

US Nationwide distribution in the states of IL & LA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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