Severity 2 of 5
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.
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.
Naturex Inc. is recalling Echinacea powder containing Azoxystrobin, a pesticide for which no tolerance is allowed.
Naturex Inc. is recalling Echinacea Agustifolia Root Powder because it contains Azoxystrobin, a pesticide for which no tolerance is allowed.
Siemens Medical Solutions USA is recalling 531 Symbia E camera systems because the collimator cart rear casters may become loose.
Dental EZ Group is recalling 45 Titan T 5K dental motors because the housing was incorrectly laser marked as a 20K motor.
Spacelabs Healthcare is recalling 8 Ultraview SL Multigas Modules because the software displays an invalid Minimum Alveolar Concentration value.
Kraft Foods is recalling Velveeta Original Pasteurized Ripe Cheese Product because a preservative ingredient was found at levels below specification.
Remel Inc. is recalling specific lots of Thermo Scientific VersaTREK REDOX 1 in vitro diagnostic products because they failed to provide positive signals for Streptococcus pneumoniae.
Pearl Valley Cheese Inc is recalling Walnut Creek Farmers Cheese because the milk used in the product tested positive for antibiotics.
Laser Peripherals LLC is recalling 25 units of DBLF-60-2 Bare Laser Fibers because a sterility expiration date was misprinted as '2016-16' instead of '2016-06'.
Zimmer, Inc. is voluntarily recalling a specific lot of dental implants due to a potential crack in the outer vial cap.
Innovasis is recalling 32 units of Excella II Standard Pedicle Screws because the size and catalog number are mislabeled.
Mt. Olive Pickle Company is recalling PepperPAK Jalapeno Slices due to undeclared sulfites. The product was distributed in Florida and New York.
Siemens Medical Solutions is updating syngo RT Dosimetrist 2.7 software to fix a safety issue where structure names were not stored correctly.
Integra LifeSciences is recalling Camino Intracranial Pressure Monitoring Kits to update labeling indicating they are unsafe in MR environments.
Teva Pharmaceuticals is recalling 1,125 blister packs of Kariva tablets because impurity test results were out of specification.
MTI Precision Products LLC is recalling 134 Lynx TM20 Torquemaster Low Speed Handpieces due to a sharp edge on the body or housing.
Axcentria Pharmaceuticals is recalling Hemo-Stat Solution because it was marketed without an approved NDA/ANDA and lacks an NDC number.
Naturex Inc. is recalling Echinacea Angustifolia Root Powder because it contains Azoxystrobin, a pesticide for which no tolerance is allowed.
New B.C.N. Trading Inc. is recalling CTF Brand Tapioca Pearl because it contains unapproved and undeclared colors. The product was distributed in MA, MD, NJ, NY, and PA.
Siemens Healthcare Diagnostics Inc is recalling six RAPIDComm Data Management Systems because the 5.0 screen layout displays incorrect test names.
Siemens Medical Solutions USA is recalling 2,458 e.cam camera systems because the collimator cart rear casters may become loose.
Codan US Corporation is recalling ColorSafe IV lines because they were manufactured and marketed prior to FDA approval.
U-Can Food Trading Inc. is recalling Crispy Taro Cookies due to undeclared dyes, including one not permitted for use.
Zimmer Manufacturing B.V. is recalling 496 bone screws because two lots were commingled and packaged with incorrect labels.
Teleflex Medical is recalling Aquapak 340 SW respiratory gas humidifier adaptors because creased packaging seals may affect integrity.