FDA recall record

Ethicon STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product code: SXPP1B430 recall — FDA Z-0047-2020

The product does not meet certain internal strength testing specifications.

Class IIclassification
Z-0047-2020official record ID
Oct 16, 2019report date

Recall record at a glance

Official recordZ-0047-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEthicon, Inc.
Report dateOct 16, 2019
Recall initiation dateAug 13, 2019
Quantity416 each
LocationSomerville, NJ, United States

Official product description

STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product code: SXPP1B430 suture

Why the product was recalled

The product does not meet certain internal strength testing specifications.

Distribution information

States: IN MD AR IL GA TN NJ PA NC CA OK CO KS UT KY WA OH OR OUS: Australia Hong King India Japan Korea Singapore Thailand United States

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

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