Recall StatusTerminated
Date Initiated2019-11-06
Date Terminated2021-11-19
Product Quantity16,380 total
Reason for Recall
There is a potential for the cuff to leak air leading to a loss of vascular occlusion.
Firm Action
Urgent Medical Device Recall Notification letters dated 11/6/19 were sent to customers.
Actions to be taken:
1. Immediately review this Recall Notification and the Business Reply Form.
2. Immediately check all stock areas and/or operating room storage for affected products. Quarantine and
discontinue use of any Color Cuff Disposable Tourniquet Cuffs identified in this Notification.
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. Return the completed BRF via fax (8665212762) 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 copies of this Notification and the BRF to all
affected locations, for each location to complete and return. Even if you have distributed all product to
another location, please complete a BRF and indicate each location that received product.
5. If the BRF for your facility indicates that recalled product is currently on hand, a shipping label will be
provided which should be used to return recalled product. Upon receipt of the recalled product, a credit
will be applied to your account.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distributions - US Nationwide distributions in the states of AL, CD, HI, IA, ID, IN, KS, KY, MA, ME, MI, MN, MT, NC, NE, NH, NJ, NV, NY, OK, OR, PA, SC, SD, TN, VA, WI, WV, and WY. Countries of Argentina, Australia, Canada, and Netherlands.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.