FDA recall record

GETINGE US SALES HEMASHIELD Knitted Double Velour Cardiovascular Fabric recall — FDA Z-1172-2018

A probable mislabeling of the product: a different-sized product is referenced on the product packaging label (i.e. 2.5 cm (width) x 7.6 cm (length))…

Class IIclassification
Z-1172-2018official record ID
Apr 4, 2018report date

Recall record at a glance

Official recordZ-1172-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGETINGE US SALES LLC
Report dateApr 4, 2018
Recall initiation dateJan 3, 2018
Quantity1
LocationWayne, NJ, United States

Official product description

HEMASHIELD Knitted Double Velour Cardiovascular Fabric

Why the product was recalled

A probable mislabeling of the product: a different-sized product is referenced on the product packaging label (i.e. 2.5 cm (width) x 7.6 cm (length)) while the actual product inside the box is 2.5 cm (width) x 15 cm (length).

Distribution information

FL

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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