FDA Device Recalls

Recalls /

#174933

Product

YNHH SCOPE KIT Kit Code: MNS10475

FDA product code
OGREar, Nose, And Throat Surgical Tray
Device class
Class 1
Medical specialty
Ear, Nose, Throat
Affected lot / code info
Lot # 2019060750 Exp 08/31/2020 Lot # 2019060450 Exp 08/31/2020 Lot # 2018110550 Exp 05/31/2020

Why it was recalled

Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer.

Root cause (FDA determination)

Material/Component Contamination

Action the firm took

1. Please identify all inventory that you have within your possession. Remove the MAJOR Nasal Decongestant from the mini-grip bag and segregate it in a location where it cannot be accessed for use. 2. Please complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter as directed. Upon receipt of this recall response, a Centurion Representative will contact you regarding retrieval of the product from your facility, if required. 3. please forward a copy of this notice to any facilities to whom this product may have been further distributed. If you have any questions, please contact (517) 546-5400 Ext 1122.

Recalling firm

Firm
Centurion Medical Products Corporation
Address
100 Centurion Way, Williamston, Michigan 48895-9086

Distribution

Distribution pattern
CT, IL

Timeline

Recall initiated
2019-06-24
Terminated
2020-07-24
Status

Source: openFDA Device Recall endpoint. Recall record ID #174933. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.