The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Medical Devices Recalls
Medical equipment, implants, and diagnostic devices
Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4 mm Diameter; Item Number: 00-2228-024-00
Zimmer Biomet
Potential failure of sterile packaging seal.
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 100 cm Length; Diameter; Item Number: 47-2490-097-01
Zimmer Biomet
Potential failure of sterile packaging seal.
There have been patient reports of abdominal hernia recurrence following hernia repair. The recalling firm has added a statement to the device's Instructions for Use to make surgeons aware of risks in using the device in Transversus Abdominis Muscle Release (TAR) procedures.
Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas c Integra AAcetaminophen150 test
Roche Diagnostics
The previous version of method sheets for the Acetaminophen assay on the COBAS INTEGRA 400 plus/800/800 CTS analyzers and the MODULAR ANALYTICS P module are missing the following statement in the Limitations-interference section: "In very rare cases, gammopathy, in particular type IgM (WaldenstrΒΏm s macroglobulinemia), may cause unreliable results."
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Zimmer Biomet
Potential failure of sterile packaging seal.
Packaging design is insufficient to prevent potential sterile barrier breach (pin hole) in Tyvek film of pouch. A limited number of previously recalled devices were inadvertently redistributed.
A previously "in specification" Finished Product with a Model 25-0657 diode had power output higher than 5 mW.
Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm Length; Item Number: 47-2255-008-01
Zimmer Biomet
Potential failure of sterile packaging seal.
There is a potential for improper welding of the yellow staple guide to the instrument. Use of a device with an improperly welded staple guide may result in improper staple formation potentially leading to bleeding or anastomotic leak.
BD VacutainerΒΏ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ΒΏ x 12 Catalog 367344
Becton Dickinson & Company
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
MicroVue SC5b-9 Plus EIA (RUO), Model A020. Research use only (RUO) product. An enzyme immunoassay for the quantitation of SC5b-9 complex present in human plasma or serum.
Diagnostic Hybrids
A component of the kit was found to contain bacterial contamination.
T4 Pullover Toga, (S/M); Catalog Number: 0400-710-000 Sterile personal protection garment
Stryker Instruments Div. of Stryker
Separation of material layers may occur, causing a potential risk of exposure to contaminants.
T4 Pullover Toga, Regular ; Catalog Number: 0400-750-000 Sterile personal protection garment
Stryker Instruments Div. of Stryker
Separation of material layers may occur, causing a potential risk of exposure to contaminants.
There is a potential for improper welding of the yellow staple guide to the instrument. Use of a device with an improperly welded staple guide may result in improper staple formation potentially leading to bleeding or anastomotic leak.
There is a potential for the connection screw of the stem extractor to break.
Customers may receive the incorrect size implant from what is labeled on the box.
Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In Vitro Diagnostic test.
Life Technologies
The lower concentration of the RNA panel could cause a NO CALL or FALSE NEGATIVE for the reporting of ROS1 fusion. If a physician relies on a false negative result, crizotinib could be improperly excluded from the patient's treatment regimen.
There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
The secondary packaging is labeled with an incorrect expiration date.