FDA recall record

Aesculap Implant Systems PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US recall — FDA Z-2579-2021

Malfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a…

Class IIclassification
Z-2579-2021official record ID
Oct 6, 2021report date

Recall record at a glance

Official recordZ-2579-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAesculap Implant Systems LLC
Report dateOct 6, 2021
Recall initiation dateApr 16, 2021
Quantity350 units
LocationCenter Valley, PA, United States

Official product description

PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13

Why the product was recalled

Malfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a potential delay in surgery

Distribution information

US Nationwide distribution in the states of FL, MI, NY, TX, WI.

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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