Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1624-2018Class II

PFR Kit- Pinnacle, Anterior Apical; Model #M0068317100. Indicated for tissue reinforcement in women with...

Boston Scientific Corporation / initiated 2018-02-12 / Terminated / root cause: design

Boston Scientific Corporation began a recall of PFR Kit- Pinnacle, Anterior Apical; Model #M0068317100. Indicated for tissue reinforcement in women with pelvic organ prolapse on . FDA classified it as Class II. As of , the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number
Z-1624-2018
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Boston Scientific Corporation
Product
PFR Kit- Pinnacle, Anterior Apical; Model #M0068317100. Indicated for tissue reinforcement in women with pelvic organ prolapse.
Product code
PWI Instrumentation, Surgical Mesh, Urogynecologic, Transvaginal Repair Of Pelvic Organ Prolapse
Root cause tag
design
FDA root cause
Device Design
Action
Boston Scientific sent Urgent Medical Device Correction letters, dated February 12, 2018, to customers via FED-EX two day delivery. Customers were informed of the updates to the affected product instructions for use and advised to read the notification carefully and immediately post the information in a visible location near the product to ensure it is easily accessible to all users of the device. Also, the notification should be passed on to any health professional of the customer's organization that needs to be aware and to any organization where the potentially affected devices have been transferred. Customers with questions should contact their local BSC (Boston Scientific) Representative. **No product is being recalled and you are not required to return product to Boston Scientific** There is no impact to previously implanted mesh devices.
Quantity in commerce
34
Distribution
Worldwide Distribution -- US, Brazil, Guatemala, Ecuador, Malaysia, Czech Republic, United Kingdom, Argentina, Honduras, Peru, Singapore, Denmark, Iceland, Chile, Nicaragua, Venezuela, Japan, Egypt, Israel, Canada, Panama, Taiwan, United Arab Emirates, Finland, Ireland, Mexico, Dominican Republic, Hong Kong, Austria, France, Italy, Costa Rica, Trinidad and Tobago, Australia, Bahrain, Georgia, Islamic Republic of Iran, El Salvador, Colombia, New Zealand, Belgium, Germany, Jordan, Norway, Russia, Pakistan, Slovakia, Portugal, South Africa, Oman, Saudi Arabia, Poland, Slovenia, Qatar, Spain, Kenya, Lebanon, Mauritius, Netherlands, Sweden, Turkey, Kuwait, Malta, Namibia, Romania, Switzerland, and Greece.
Product codes and lots
GTIN: 08714729773047  Batch numbers:  ML00002841

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1624-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1616-2018Class IITerminatedVoluntary: Firm initiated
Z-1617-2018Class IITerminatedVoluntary: Firm initiated
Z-1618-2018Class IITerminatedVoluntary: Firm initiated
Z-1619-2018Class IITerminatedVoluntary: Firm initiated
Z-1620-2018Class IITerminatedVoluntary: Firm initiated
Z-1621-2018Class IITerminatedVoluntary: Firm initiated
Z-1622-2018Class IITerminatedVoluntary: Firm initiated
Z-1623-2018Class IITerminatedVoluntary: Firm initiated
Z-1624-2018Class IITerminatedVoluntary: Firm initiated
Z-1625-2018Class IITerminatedVoluntary: Firm initiated
Z-1626-2018Class IITerminatedVoluntary: Firm initiated