“bacteriostatic water” matches in 13 of 26 searchable datasets. 13 did not answer this time (Device classification, 510(k) clearances, PMA approvals, Establishments and listings, Device adverse event reports (MAUDE), COVID-19 serology test evaluations, Cosmetic adverse event reports, Food recalls, Food and supplement adverse event reports (CAERS), Animal drug adverse event reports, Tobacco product problem reports, UNII codes, Complete response letters); try again shortly.
Medtronic, Inc. - Neuromodulation · This letter provides important reminders concerning the potential for a pocket fill during a SynchroMed II or SynchroMed EL implantable drug pump refill proced…
Medtronic Neuromodulation · Medtronic issued a letter to healthcare professionals providing important safety information regarding MRI (magnetic resonance imaging) effects on SynchroMed E…
Medtronic Neuromodulation · Medtronic issued a letter to healthcare professionals providing important safety information regarding MRI (magnetic resonance imaging) effects on SynchroMed E…
MEDLINE IND · Product was not sterilized. Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a 3rd party shippin…
U. S. DEPARTMENT OF HEALTH, EDUCATION AND WELFARE v PUBLIC HEALTH SERVICE FOOD AND DRUG ADMINISTRATION _ Rockvifle, Maryland 20852 NEWS Donald Berreth: 301 443-3285 ’ v Home Phone: 301_ 869-1795 72—8‘ 'FOR RELEASE : ’ ll…
Press release35 pages
U. S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Food and Drug Administration Washington 25, D. C.
I~‘ 4 ‘3‘“ BROOKS WO-Z-4171 U. S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Food and Drug Administration Washington 25, D. C. F02 men IN AJ‘I. PAIERS I'm-£36 Saturday, March 7, 1961; Promotion and nationwidB sale by…
Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.