Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2182-2020Class II

Osteovationex 5Cc Inject Formula. Ref/udi: 390-0005/00813845020023 -

Osteomed / initiated 2020-04-02 / Terminated / root cause: supplier

Osteomed, LLC began a recall of OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the... on . FDA classified it as Class II and gives the reason as "Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration". As of , the recall status on record is Terminated, and MDM tags the root cause as supplier.

Recall record

Recall number
Z-2182-2020
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Osteomed
Product
OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Product code
MQV Filler, Bone Void, Calcium Compound
Reason for recall
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
Root cause tag
supplier
FDA root cause
Vendor change control
Action
On 04/02/2020, an URGENT Medical Device Recall letter was sent to all consignees affected by the recall. OsteoMed has requested that affected customers: (1) review this letter in full, review current inventory, and complete and return the Acknowledgement and Receipt Form via email or fax; and (2) return unused inventory via Federal Express (using OsteMed account)
Quantity in commerce
647
Distribution
Worldwide distribution - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA. MA, MD, ME. MI, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and WY and the countries of AUSTRALIA, ITALY, KOREA, MALAYSIA, PERU, SINGAPORE and THAILAND.
Product codes and lots
LOT 1128523, 1129958, 1135746, 1142073, 17071104, 17100404 and 1126669

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2182-2020
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2180-2020Class IITerminatedVoluntary: Firm initiated
Z-2181-2020Class IITerminatedVoluntary: Firm initiated
Z-2182-2020Class IITerminatedVoluntary: Firm initiated
Z-2183-2020Class IITerminatedVoluntary: Firm initiated
Z-2184-2020Class IITerminatedVoluntary: Firm initiated
Z-2185-2020Class IITerminatedVoluntary: Firm initiated
Z-2186-2020Class IITerminatedVoluntary: Firm initiated
Z-2187-2020Class IITerminatedVoluntary: Firm initiated
Z-2188-2020Class IITerminatedVoluntary: Firm initiated
Z-2189-2020Class IITerminatedVoluntary: Firm initiated
Z-2190-2020Class IITerminatedVoluntary: Firm initiated
Z-2191-2020Class IITerminatedVoluntary: Firm initiated