Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot of Hannaford Supermarkets TASTE OF INSPIRATIONS GREEK PASTA SALAD Net Wt. 10 oz. (284g) because it may contain…
GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
Product may contain undeclared milk.
Don's Salads is recalling Magnum Shrimp Salad due to undeclared milk. An ingredient, used in the manufacture of the salads, has been recalled due to undeclared milk.
Presence of Foreign Substance: possibility of the presence of metal in the product.
Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation…
Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
CGMP Deviations: Lack of quality assurance at the API manufacturer.
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
GMP Deviations; FDA inspection found significant manufacturing practices that call into question the safety, identity, strength, quality and purity of unexpired drug products manufactured…
The Access immunoassays are susceptible to biotin interference.
Linear performance information in product insert does not match that listed in the approved premarket notification
Cracks may occur over time on the tube holding shaft near the base of the tube mounting flange.
There are potential issues with results reporting for certain run-based tests. Under certain conditions, the wrong results could inadvertently be verified.
Under certain conditions, the cables used with the Hemo system during a patient procedure could stop displaying the patient SpO2 causing a slight delay in patient care.
The incorrect Loctite adhesive was used to assemble the impactor heads.
Cotton tip of the device may disengage due to insufficient adhesive
Carestream found a single unit where four screws in the assembly were not applied in the manufacturing process. This could result in separation of the tube and yoke assembly.
Under certain conditions, the cables used with the Hemo system during a patient procedure could stop displaying the patient SpO2 causing a slight delay in patient care.
The Access immunoassays are susceptible to biotin interference.
Browse recent months with enough recall history for useful comparison.
