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Terminated

T4 Pullover Toga, X-Large; Catalog Number: 0400-770-000 Sterile personal protection garment

FDA Recall Z-1504-2018 · Posted None

Recall StatusTerminated
Product CodeFYA
Date Initiated2018-02-23
Date Terminated2019-05-23
Product Quantity34570 total products

Reason for Recall

Separation of material layers may occur, causing a potential risk of exposure to contaminants.

Firm Action

On March 7, 2018 Stryker Instruments mailed Urgent Medical Device Recall Notifications to affected customers. Distributors and Sales Representative were notified via e-mail. Customers were instructed to: 1) Immediately review this Recall Notification; 2) Immediately check all stock areas and/or operating room storage for affected products. Quarantine and discontinue use of any affected T4 and T5 Togas; 3) Complete the enclosed Business Reply Form (BRF) to confirm receipt of this Notification and identify how many affected items are currently in your inventory. Please complete and return the BRF even if you dont have any affected product on hand. Fax the completed BRF to Stryker Instruments at 866-521-2762, or email to [email protected]. Note: Your signature on the BRF indicates that you received and understand this Notification and have followed the instructions in the Notification; 4) If you have further distributed this product, please forward this Notification and the attached BRF to all affected locations. Please indicate each location on the BRF; 5) If the BRF for your facility indicates that recalled product is currently on hand, a FedEx label will be emailed to you and should be used to return recalled product. Upon receipt of the recalled product, a credit will be issued to your account. Customer with questions or concerns may call (800)253-3210.

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide and Ireland, Japan, South Korea, UK

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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