How many recalls does Ortho Development Corporation have?

Recalert has 7 U.S. recalls on record for Ortho Development Corporation, published between May 21, 2014 and May 13, 2020.

What was the most recent Ortho Development Corporation recall?

FDA recall Z-1903-2020, published May 13, 2020: Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.

Ortho Development Corporation appears as the recalling firm in recalls from: FDA (7).

Recalls filed with 1 agency: FDA (7).

First recall on record: May 21, 2014. Most recent: May 13, 2020.

Risk classification: Class II: 7

Date	Agency	Product	Recall number
May 13, 2020	FDA	Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.Z-1903-2020	Z-1903-2020
August 27, 2014	FDA	PS Tibial Insert, REF 163-1XXX Product Usage: UHMWPE component used in TKA procedures…Z-2255-2014	Z-2255-2014
August 27, 2014	FDA	Tibila Insert CK, Balanced Knee System Revision, REF563-1YYY Product Usage: UHMWPE com…Z-2257-2014	Z-2257-2014
August 27, 2014	FDA	Pivot Bipolar Cup 22x42/43-51/53mm, REF 133-YYYY Product Usage: Used in a hemiarthrop…Z-2253-2014	Z-2253-2014
August 27, 2014	FDA	Patella 38mm, REF164-0038 Product Usage: UHMWPE component used in a TKA procedure to…Z-2254-2014	Z-2254-2014
August 27, 2014	FDA	Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component u…Z-2256-2014	Z-2256-2014
May 21, 2014	FDA	PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee Sys…Z-1610-2014	Z-1610-2014

How many recalls does Ortho Development Corporation have?: Recalert has 7 U.S. recalls on record for Ortho Development Corporation, published between May 21, 2014 and May 13, 2020.
What was the most recent Ortho Development Corporation recall?: FDA recall Z-1903-2020, published May 13, 2020: Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.
Which agencies have handled Ortho Development Corporation recalls?: Ortho Development Corporation appears as the recalling firm in recalls from: FDA (7).

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