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.
Paleteria La Jalpita is recalling pineapple popsicles in Oregon and Washington due to undeclared Yellow No. 5 and Yellow No. 6.
The Apothecary Shoppe is recalling SIU-Tri-Mix 24/1/20 Injection vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.
Roche is recalling S2 Fluid Packs for the Cobas b 221 system because they may generate a transponder error, preventing the instrument from starting measurements.
The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 17/0.6/5.7 Injectable in Oklahoma due to lack of assurance of sterility from missing environmental monitoring documentation.
The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentermine Injection due to a lack of documentation proving proper environmental monitoring during production.
GE Healthcare is recalling 82 MRI scanners because a missing spacer may cause images to be flipped left-right with incorrect orientation annotations.
Paleteria La Jalpita is recalling Pistachio-Pistache popsicles due to undeclared Yellow No. 5. The product was distributed in Oregon and Washington.
Church & Dwight is recalling Lil Critters Gummy Vites Complete Multivitamin because two lots were produced using Adult Multivitamin bulk.
The Apothecary Shoppe is recalling SIU-Tri-Mix vials because documentation for environmental monitoring during production was missing, raising concerns about sterility.
The Apothecary Shoppe LLC is recalling SIU-Phentolamine 5 mg/mL vials in Oklahoma due to lack of documentation for environmental monitoring during production.
The Apothecary Shoppe LLC is recalling SIU-Papaverine 30 mg/mL Injection due to a lack of documentation ensuring proper environmental monitoring during production.
Victor's Market Company is recalling approximately 7,368 pounds of chicken products because they were slaughtered under religious exemption, which was not declared on the label.
The Anspach Effort, Inc. is recalling 95 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.
EXP Pharmaceutical Services Corp is recalling 10 units of Medical Device Exchange Surgical Gowns because the company failed to register as a medical device establishment or establish a quality system.
Boehringer Ingelheim is recalling 358,647 Combivent Respimat inhalers because the delivery system may fail to spray properly.
The Anspach Effort, Inc. is recalling 91 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.
Dairy Farmers of America is recalling Borden Fat Free Sharp Cheddar cheese because a piece of plastic film strip might remain attached to the cheese slice.
The Anspach Effort, Inc. is recalling 142 G1 dissection tools because the labeled shaft exposure may not be consistent with all listed attachments, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 110 Anspach Fluted Barrel dissection tools because the specified shaft exposure may be inconsistent with attachments, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 69 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.
Dairy Farmers of America is recalling Borden 2% Pepper Jack White cheese because plastic film strips may remain attached to the slices.
The Anspach Effort, Inc. is recalling 75 Anspach 7mm Extra Coarse Diamond Ball dissection tools because the specified shaft exposure may be inconsistent with the labeled attachments.
Siemens is recalling ACUSON S2000 and S3000 ultrasound systems with Virtual Touch IQ due to a potential measurement alignment error.
Dairy Farmers of America is recalling Meijer Monterey Pepper Jack cheese slices because a piece of plastic film might remain attached to the cheese.
The Anspach Effort, Inc. is recalling 88 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.