Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to failure to meet product specifications.
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Surgical Instruments
🏥 Medical Devices • 6,839 recalls
Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Teleflex Medical
Class I - Dangerous
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
Class I - Dangerous
Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
Class I - Dangerous
Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.
Products from the identified lots may exhibit difficulty in removing the protective balloon sheath which can result in issues with inflating or deflating the balloon.
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Molnlycke Health Care
Class I - Dangerous
Sterilization validation failure.
Class I - Dangerous
Product's non-conformity involves the integrity of the seal in the sterile packaging. It is possible that the seal on the sterile packaging has been compromised resulting in a loss of sterility of the medical device contained within.
Class I - Dangerous
Complaints concerning kinked haptics that were occurring during lens delivery.
Class I - Dangerous
Product's non-conformity involves the integrity of the seal in the sterile packaging. It is possible that the seal on the sterile packaging has been compromised resulting in a loss of sterility of the medical device contained within.
Class I - Dangerous
Product's non-conformity involves the integrity of the seal in the sterile packaging. It is possible that the seal on the sterile packaging has been compromised resulting in a loss of sterility of the medical device contained within.
Class I - Dangerous
Products from the identified lots may exhibit difficulty in removing the protective balloon sheath which can result in issues with inflating or deflating the balloon.
Class I - Dangerous
Product's non-conformity involves the integrity of the seal in the sterile packaging. It is possible that the seal on the sterile packaging has been compromised resulting in a loss of sterility of the medical device contained within.
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Biomet Microfixation
Class I - Dangerous
Part of the number on the tray lid differ from the part number on the base.
Class I - Dangerous
Products from the identified lots may exhibit difficulty in removing the protective balloon sheath which can result in issues with inflating or deflating the balloon.
White OR Towels, X-Ray Detectable, Sterile, 4 Towels per/pk; 20pk/Cs. Intended for packing and absorption externally or within patient wounds in various procedures or surgical cases.
Medical Action Industries
Class I - Dangerous
Lint present on sterile Operating Room Towels.