Lack of Assurance of Sterility; media fill failure at manufacturer
All Recalls
95,083 total recalls in our database
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per Bottle, Rx only, Distributed By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5721-56
Teva Pharmaceuticals USA
Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Lack of Assurance of Sterility; media fill failure at manufacturer
Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA Made in USA, NDC 62032-222-02
Valeant Pharmaceuticals North America
Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy Night Cream is being recalled due to incomplete packaging/labeling. The bottle is missing the product insert and outer carton which contain the complete instruction for use and safety information.
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.
Install CD, Spine tools, Plus and S7, Version 25. Model Number 9731958.
Medtronic Navigation
Software issue related to the StealthStation S7 system and the Synergy Spine application Version 2.1 configured with Spine Tool Install CD version 25. Issue may result in user being unable to navigate the Navigated Elevate Inserter with the StealthAiR Spine Frame during spine surgical procedures.
Penumbra has identified an issue in these four lots involving a raw material component of the delivery wire. This issue could result in breakage of the delivery wire, which could potentially lead to serious patient injury or death.
BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
Becton Dickinson & Company
BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.
It was discovered that all five microwave ovens fail to have concealed or inaccessible safety interlocks.
An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
When the user has not set up any user preference on the sorting order to render the study images (OS/OD/etc.) and reports, the ECP may get an incorrect study index. If the user attempts to delete an image, ECP may then read that image as OS when it is, in fact, OD.