Complete FDA and NHTSA recall records dated in 2018, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Gel Spice, Inc. is recalling three beef flavored bouillon cube products because they contain undeclared allergens -- soy and wheat.
Product may be contaminated with Listeria monocytogenes.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.
Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Presence of foreign substance: metallic razor blade was found in one bottle.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
Subpotent Drug
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Presence of foreign substance: The recall was initiated due to black particles being observed while performing routine post-release stability testing on Mefenamic acid capsules
Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
Microbial Contamination of Non Sterile Product; presence of yeast and potential B. cepacia contamination
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Potential for leak test failures.
The Locking Punch Guide was not sufficiently guiding the large press fit punch, causing the implant to be placed 2-3mm more posterior than intended.
The tube adapter-plate green/yellow protective earthing (PE) wire was removed. and spacers with different thickness were used to position pre-loc ring in respect to focal spot in specified…
The Locking Punch Guide was not sufficiently guiding the large press fit punch, causing the implant to be placed 2-3mm more posterior than intended.
The syringe plunger grippers may fail to automatically close around the syringe plunger press when the gripper control knob has been closed.
OrthoScan Inc. discovered during investigation of a non-standard work flow a non-conformity of the devices. Specifically, the system software allows a user to activate the Digital Zoom…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
