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CME America Updates Recall of BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion

Murilo Freitas - 04:00, 4 de agosto de 2020587
CME America BodyGuard® Infusion System Administration Sets because the pumps may have a slower than expected delivery of medication (under-infusion), or faster than expected delivery of medication (over-infusion) or a delay in therapy.

http://www.fda.gov/medical-devices/medical-device-recalls/cme-america-updates-recall-bodyguard-infusion-pump-system-due-risk-over-and-under-infusion

 
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Roque Plast S.A. de C.V. Issues Voluntary Nationwide Recall of Command Brands Gel AntiBac Instant Hand Sanitizer Lots 200371-12, 200371OH-05, 170420OH-06, 170420OH-8 Due to Potential Presence of Methanol (Wood Alcohol)

Murilo Freitas - 04:00, 3 de agosto de 2020679
Roque Plast S.A. de C.V. is voluntarily recalling lots 200371-12, 200371OH-05, 170420OH-06, 170420OH-8 manufactured by Roque Plast S.A. de C.V. of Command Brands Gel AntiBac Instant Hand Sanitizer to the consumer level. This recall has been initiated due purported potential presence of methanol indi

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/roque-plast-sa-de-cv-issues-voluntary-nationwide-recall-command-brands-gel-antibac-instant-hand

 
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LABORATORIOS JALOMA S.A. de C.V. Issues Voluntary Recall of the Jaloma Antiseptic Hand Sanitizer Due to the Potential Presence of Undeclared Methanol

Murilo Freitas - 04:00, 31 de julio de 2020531
LABORATORIOS JALOMA S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of the Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% With vitamin E to the consumer level. This recall has been initiated because FDA sampled the 500 mL product and found it to be contaminated with undeclar

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/laboratorios-jaloma-sa-de-cv-issues-voluntary-recall-jaloma-antiseptic-hand-sanitizer-due-potential

 
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