💊 Drugs Class I - Dangerous
Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
Kimberly-Clark
19 recalls • • Categories: Other Drugs, Other Medical Devices, Infusion Pumps, Surgical Instruments, Diagnostic Equipment
🏥 Medical Devices Class I - Dangerous
Potential for tampon to come apart upon removal.
🏥 Medical Devices Class I - Dangerous
Potential for tampon to come apart upon removal.
🏥 Medical Devices Class I - Dangerous
Potential for tampon to come apart upon removal.
🏥 Medical Devices Class I - Dangerous
Potential for tampon to come apart upon removal.
🏥 Medical Devices Class I - Dangerous
Product may contain a cannula with an active tip length of only 5mm rather than 10mm as indicated on the label.
🏥 Medical Devices Class I - Dangerous
Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7 mL Epilor plastic Luer-Lok LOR Syringes under recall by Becton Dickinson (BD) because the product may stall or stick when traveling within the barrel of the syringe.
🏥 Medical Devices Class I - Dangerous
Some individual container filter units might contain thin areas that may potentially compromise the ability of the filter to maintain a sterile barrier.
🏥 Medical Devices Class I - Dangerous
Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately.
🏥 Medical Devices Class I - Dangerous
Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
🏥 Medical Devices Class I - Dangerous
Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
🏥 Medical Devices Class I - Dangerous
The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
🏥 Medical Devices Class I - Dangerous
The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
🏥 Medical Devices Class I - Dangerous
The impacted product was not intended for commercial distribution to end users.
🏥 Medical Devices Class I - Dangerous
A defect of the "fuse holder" can lead to a Control Unit failure that may cause the device to lose its ability to warm and maintain set temperature and may also result in excessive heat with the fuse assembly that could lead to the generation of smoke.
Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.
Complaints were received of gowns pilling or balling, linting and abrades, blood strikethrough and fibers falling off the gowns.
💊 Drugs Class I - Dangerous
Microbial Contamination of Non-Sterile Products; The affected lots were found to be contaminated with bacterium, Burkholderia cepacia complex.
💊 Drugs Class I - Dangerous
Microbial Contamination of Non-Sterile Products; The affected lots were found to be contaminated with bacterium, Burkholderia cepacia complex.