Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, a component of the Trinity Acetabular System. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, a component of the Trinity Acetabular System.
Brand
Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
The affected products are shipment specific and were delivered to the consignee between 7/22-26/2021. Lot number 441120 was delivered to the consignee 7/23/2021 and 7/26/2021.
Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom is recalling Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, due to The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination o. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
Recommended Action
Per FDA guidance
On 7/28&29/2021, the firm sent emails entitled "IMPORTANT-containment request FA COUK 2021 013" which notified the consignee they have been identified as receiving one or more of the medical devices listed in the attached Excel file due to them potentially having physical and/or water damage. They were to quarantine the parts until further instructions were issued. On 9/7/2021, Corin USA issued recall letters dated 9/3/2021 via email on 9/7/2021 requesting the devices be quarantined and returned.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026