Consumer Product Safety Commission announced the following voluntary recalls on Nov. 14:
The Food and Drug Administration on Nov. 14 issued a new guidance document on procedures for reviewing FDA denials of export certificates for medical devices. The guidance document details the process for exporters to correct deficiencies that caused FDA to deny issuance of a Certificate to Foreign Government (CFG) for a device, as well as for requesting agency review of denials.
Consumer Product Safety Commission announced the following voluntary recalls on Nov. 12:
Consumer Product Safety Commission announced the following voluntary recalls on Nov. 6:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 31:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 29-30:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 22:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 10:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 8:
Consumer Product Safety Commission announced the following voluntary recalls on Oct. 4: