State
73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Instrumentation Laboratory is recalling 8,0319 kits of HemosIL Normal Control 1 UNASSAYED because the product lacks FDA 510(k) approval.
National Enzyme Co is recalling bulk digestive enzyme powder that may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling Bulk C665 powder because it may contain chloramphenicol levels exceeding 0.3 ppb. The product was distributed domestically and internationally.
National Enzyme Co is recalling Cellulase Cellulolytic Enzymes because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above permitted limits. The product is distributed domestically and internationally.
National Enzyme Co is recalling 1.7 million Supergest bulk capsules because they may contain chloramphenicol above the 0.3 ppb limit.
National Enzyme Co is recalling bulk dietary supplement powders that may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling specific lots of Gluten & Dairy Digest enzyme supplements because they may contain chloramphenicol above 0.3 ppb.
Biomet, Inc. is recalling 21 CurvTek Eye Needles because the inner label incorrectly identifies the product size and reference number.
National Enzyme Co is recalling Wellzymes Gastric Ease enzyme supplements because a raw material may contain chloramphenicol levels above 0.3 ppb.
CooperVision is recalling 153 cartons of Pro Clear 1 Day Sphere contact lenses because the outer cartons display incorrect expiration dates, although the inner blisters are correct.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above the permitted limit.
National Enzyme Co is recalling 9326 Kirkman Bacterial Bio 6 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Bulk B199 Reviva Digestion Bulk powder because it may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling BioSan Labs Hi Potency capsules because the raw material may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling bulk Digest Platinum capsules because they may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling TriEnza digestive enzyme supplements because they may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling Wellzymes enzyme supplements because a raw material may contain chloramphenicol above the 0.3 ppb limit.
National Enzyme Co is recalling NWC Naturals dietary supplements because a raw material may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling Heryben and Bulk C269 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Karl Storz Endoscopy America is recalling specific flexible intubation fiberscopes because the suction channel material is incompatible with STERRAD sterilization systems.