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.
Teva Pharmaceuticals is recalling 40,750 dispensers of Jolessa contraceptive tablets because some packages may be missing placebo tablets.
App Pharmaceuticals is recalling specific lots of Heparin Lock Flush Solution because of incomplete documentation associated with test results.
Tripath Imaging is recalling Manual Method 1: 480 Test Kits because the PrepStain Syringing Pipettes may leak and fail to dispense the minimum required volume.
Hospira, Inc. is recalling 164,568 containers of Magnesium Sulfate in Water for Injection because the product contained higher levels of magnesium sulfate than specified.
Tripath Imaging is recalling PrepStain Syringing Pipettes because they may leak and fail to dispense the minimum required volume of 7.5 mL.
Quadrant Chemical Corporation is recalling DermaZinc Spray because the product is subpotent and does not meet the labeled 0.25% zinc pyrithione level.
Integra LifeSciences Corp. is recalling Integra Mozaik Strip units because the Instructions for Use contain incorrect Spanish and French translations of the term "bone marrow aspirate."
Bumble Bee International is recalling 318,735 cases of Fancy Whole Oysters due to potential contamination from insanitary conditions.
King & Prince Seafood is recalling Mrs. Friday's Chef Dusted Pacific Oysters because they were prepared or held under insanitary conditions, potentially rendering them injurious to health.
Integra LifeSciences Corp. is recalling 42 units of Mozaik Putty because the Instructions for Use contain incorrect Spanish and French translations of the term 'bone marrow aspirate'.
Crown Prince Inc is recalling canned oysters because they were prepared under insanitary conditions that may have rendered them injurious to health.
Tomberlin Automotive Group is recalling 2012 AVL low-speed vehicles because seat belt tags lack the date of manufacture, failing federal safety standards.
Winnebago is recalling 2012 Era motor homes because they have the wrong vehicle weight label, failing to comply with federal safety standards.
Winnebago is recalling certain 2010-2011 Tour and Itasca Ellipse motor homes because they have labels indicating the wrong type of load range tires.
Setra is recalling 97 S417 and S417 TC motor coaches because the partition glass behind the driver lacks required DOT markings.
Fleetwood is recalling specific 2010-2011 motor homes because the federal certification tag lists incorrect front and rear tire PSI values.
BMW is recalling 2009-2010 7-Series and 2010 550i Gran Turismo vehicles because the tire pressure label incorrectly lists a seating capacity of five instead of four.
Gulf States Toyota is recalling 2005-2010 Toyota and Scion vehicles sold without required tire load capacity labels.
Fleetwood is recalling 2009 and 2010 Terra and Fiesta Class A motor homes because the certification and cargo capacity tags are incorrect.