FDA recall record

American Contract Systems Sterile Custom Packs to be used in surgical procedures recall — FDA Z-2174-2020

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Class IIclassification
Z-2174-2020official record ID
Jun 10, 2020report date

Recall record at a glance

Official recordZ-2174-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmerican Contract Systems
Report dateJun 10, 2020
Recall initiation dateApr 13, 2020
Quantity2868 total kits
LocationZelienople, PA, United States

Official product description

Sterile Custom Packs to be used in surgical procedures.

Why the product was recalled

The surgical gowns were manufactured in a facility that is not registered by the FDA.

Distribution information

US Nationwide distribution including in the state of Pennsylvania.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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