FDA recall record

Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER recall — FDA Z-1290-2021

The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the…

Class IIclassification
Z-1290-2021official record ID
Mar 31, 2021report date

Recall record at a glance

Official recordZ-1290-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCorin Ltd
Report dateMar 31, 2021
Recall initiation dateJan 25, 2021
Quantity23 units
LocationCirencester, N/A, United Kingdom

Official product description

Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit, titanium alloy shell; acetabular liners in neutral offset, +4mm offset, +4mm oblique, neutral 4mm EPW; and ceramic and CoCrMo modular heads. The ceramic and CoCrMo modular heads are compatible with Corin titanium femoral stems. The Trinity Biolox Ceramic heads are packaged in a double peel pouch configuration.

Why the product was recalled

The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa.

Distribution information

Worldwide distribution - US Nationwide distribution and the countries of Colombia, Poland, Germany, Australia.

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: E-Mail.

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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