FDA recall record

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and recall — FDA Z-1689-2024

Product was distributed in the United States without proper regulatory approval.

Class IIclassification
Z-1689-2024official record ID
May 1, 2024report date

Recall record at a glance

Official recordZ-1689-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBaxter Healthcare Corporation
Report dateMay 1, 2024
Recall initiation dateMar 15, 2024
Quantity165 units
LocationDeerfield, IL, United States

Official product description

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery

Why the product was recalled

Product was distributed in the United States without proper regulatory approval.

Distribution information

US Nationwide distribution in the states of LA, GA, IN, VA FL, NY, CA.

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: Letter.

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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