510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1080-2018Class II

General Purpose Instrument Tray

Centurion Medical Products, LP / initiated 2017-10-23 / Terminated / root cause: manufacturing process

Centurion Medical Products Corporation began a recall of GENERAL PURPOSE INSTRUMENT TRAY on . FDA classified it as Class II and gives the reason as "Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1080-2018
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Centurion Medical Products, LP
Product
General Purpose Instrument Tray
Product code
LRP Tray, Surgical
Reason for recall
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
On October 16, 2017 a PRODUCT CORRECTION letter was issued to customers notifying them that if they had any kits in their inventory, Centurion will supply labels to affix to the front of each kit instructing the user to discard the prep pad upon opening the kit. Other components of the kit may continue to be used and are NOT within the scope of this recall.
Distribution
Nationally
Product codes and lots
75121 75175 71435 75455 75690 SR245  Lot codes: 2017071990 2016110990 2016040790  2017022090 2016112490 2017010390 2017082390 2015101290 2015111790 2016032290 2016051790 2016053090 2016102490 2017013190 2017032990 2017080290 2015110390 2016010490 2016012090 2016020890 2016041890 2016061390 2016090590 2016110790 2017010990 2017021390 2017032190 2015092190 2015120190 2015121490 2016022590 2016120190 2017010390 2017011090 2015093090 2015112390 2016020390 2016092290 2016091590

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1080-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1078-2018Class IITerminatedVoluntary: Firm initiated
Z-1079-2018Class IITerminatedVoluntary: Firm initiated
Z-1080-2018Class IITerminatedVoluntary: Firm initiated
Z-1081-2018Class IITerminatedVoluntary: Firm initiated
Z-1082-2018Class IITerminatedVoluntary: Firm initiated
Z-1083-2018Class IITerminatedVoluntary: Firm initiated
Z-1084-2018Class IITerminatedVoluntary: Firm initiated
Z-1085-2018Class IITerminatedVoluntary: Firm initiated
Z-1086-2018Class IITerminatedVoluntary: Firm initiated
Z-1087-2018Class IITerminatedVoluntary: Firm initiated
Z-1088-2018Class IITerminatedVoluntary: Firm initiated
Z-1089-2018Class IITerminatedVoluntary: Firm initiated
Z-1090-2018Class IITerminatedVoluntary: Firm initiated
Z-1091-2018Class IITerminatedVoluntary: Firm initiated
Z-1092-2018Class IITerminatedVoluntary: Firm initiated
Z-1093-2018Class IITerminatedVoluntary: Firm initiated
Z-1094-2018Class IITerminatedVoluntary: Firm initiated
Z-1095-2018Class IITerminatedVoluntary: Firm initiated
Z-1096-2018Class IITerminatedVoluntary: Firm initiated
Z-1097-2018Class IITerminatedVoluntary: Firm initiated
Z-1098-2018Class IITerminatedVoluntary: Firm initiated