Severity 1 of 5
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Severity 1 (Low) recalls are typically cosmetic defects, documentation issues, packaging-only problems, and Class III administrative corrections. The product itself is unlikely to cause adverse health consequences. The manufacturer is correcting the issue to comply with FDA or USDA rules, not because anyone is at risk. You can almost always continue using a Severity-1 product without concern.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
The Binding Site Group is recalling Optilite IgG4 Kits because the product insert does not reflect a change to the measuring range.
Actavis Inc is recalling specific lots of Albuterol Sulfate Inhalation Solution because the product failed impurity specifications for a known degradant.
GE Healthcare is updating user documentation for OEC 9900 Elite surgical carts to clarify maintenance and component replacement frequencies.
GE Healthcare is updating user documentation for OEC 9800 surgical tables to clarify maintenance and component replacement schedules.
Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.
Atlas Meat Company is recalling pork sausage products because they may contain monosodium glutamate (MSG), which is not declared on the label.
Piazza Produce is recalling 283 units of Hickory Smoke salt because the product labeling does not contain a listing of ingredients.
Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.
Piazza Produce, Inc. is recalling various sizes of Garlic Salt because the product labeling does not contain a listing of ingredients.
Pharm D Solutions is recalling Testosterone Cypionate 200 mg/mL vials because the label incorrectly lists grapeseed oil instead of sesame oil.
Piazza Produce, Inc. is recalling 197 units of pumpkin pie spice because the product labeling does not contain a listing of ingredients.
Piazza Produce, Inc. is recalling 701 units of taco seasoning because the product labeling does not contain a listing of ingredients.
Piazza Produce, Inc. is recalling specific lots of BBQ Spice because the product labeling does not contain a listing of ingredients.
Piazza Produce, Inc. is recalling 715 units of blackened seasoning because the product labels do not list ingredients. The recall covers food service establishments in five states.
Piazza Produce, Inc. is recalling celery salt products because the packaging does not list ingredients. The recall affects food service establishments in five states.
Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.
Philips Medical Systems is recalling one Brilliance iCT system because the installation of four M12 bolts was not correctly documented.
Piazza Produce, Inc. is recalling seafood seasoning products because the labels do not list ingredients. This affects food service establishments in five states.
Piazza Produce, Inc. is recalling 44 units of Bayside Seasoning because the product labeling does not contain a listing of ingredients.
Piazza Produce, Inc. is recalling onion salt in various sizes because the product labeling does not contain a listing of ingredients.
Vintage Pharmaceuticals is recalling 1,200 bottles of Temazepam 7.5 mg capsules because they failed stability specifications. The affected lot is distributed nationwide.
Sterling Diagnostics is recalling 165 Colorimetric SGOT diagnostic kits because previously extended expiration dates were rescinded.
Sterling Diagnostics is recalling 173 Enzymatic Uric Acid diagnostic kits because previously extended expiration dates were rescinded.
Sterling Diagnostics is recalling 97 units of Enzymatic Cholesterol diagnostic kits due to a revision of previously extended expiration dates.
Sterling Diagnostics is recalling Serum Iron/IBC diagnostic kits because previously extended expiration dates were rescinded.