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.
Siemens is recalling nine Mobilett Mira mobile x-ray systems because a loose center screw on the driving wheel may cause the system to become immobilized.
Dr Pepper/Seven Up is recalling Stewart's Diet Orange N' Cream Soda because the ingredient label lists ingredients for the regular version.
Princeton Biomeditech is recalling Orasure QuickFlu Rapid A+B Test kits due to reports of dual positive results for Flu A and Flu B.
Apio Inc. is recalling specific lots of broccoli, cauliflower, and peas because they may contain small plastic shavings from a production line.
Breg Inc. is recalling Polar Dressing units that are thinner than specified, making them less durable and prone to tearing.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Multi-Diluent 1 because it may show decreased dilution recovery when stored on-board the system.
Drucker Labs is recalling intraKID Lot 658 because it was manufactured with an incorrect form of Vitamin B3, which may cause temporary skin symptoms.
Princeton Biomeditech is recalling 90 kits of the Status Flu A + B Test due to reports of dual positive results.
Becton Dickinson & Co. is recalling 57 kits of the BD GeneOhm Cdiff Assay because of leakage in Cepheid SmartCycler reaction tubes.
Becton Dickinson & Co. is recalling 68 kits of the BD GeneOhm MRSA ACP Assay due to leakage in Cepheid SmartCycler reaction tubes.
Clif Bar and Company is recalling Blueberry Crisp CLIF Bars because some were mistakenly packaged in Chocolate Chip wrappers.
Clif Bar is recalling White Chocolate Macadamia bars because they contain undeclared coconut. The error occurred when Coconut Chocolate Chip bars were placed in the wrong wrappers.
Capintec is recalling Captus 3000 Thyroid Uptake Systems with specific software revisions due to a potential error in the 'Measure Liquid and Subtract Residual' protocol.
Princeton Biomeditech Corp is recalling 103 kits of the Poly stat Flu A & B Test due to reports of dual positive results.
Clif Bar and Company is recalling Coconut Chocolate Chip bars due to undeclared coconut in the ingredient statement.
Becton Dickinson & Co. is recalling 32 kits of the BD GeneOhm Cdiff Assay because reaction tubes may leak. The product is distributed nationwide.
Becton Dickinson & Co. is recalling 38 kits of the BD GeneOhm MRSA ACP Assay due to leakage in Cepheid SmartCycler reaction tubes.
Becton Dickinson is recalling BD GeneOhm VanR Assay kits because reaction tubes may leak. The recall affects 5 kits distributed nationwide.
Toshiba American Medical Systems Inc. is recalling three MRI systems due to a potential problem with the position of the hold in the lug terminals on power cables.
Clif Bar and Company is recalling 4,608 Chocolate Chip CLIF Bars because some Blueberry Crisp bars were mistakenly placed in Chocolate Chip wrappers.
Medtech Products Inc. is recalling Little Remedies For Tummys Stimulant Laxative Drops because the sennosides ingredient is subpotent.
Apio Inc. is recalling specific fresh vegetables due to potential contamination with small plastic shavings from a production line.
Apio Inc. is recalling specific lots of Brussels sprouts, broccoli-cauliflower, and snap peas due to potential foreign material contamination from small plastic shavings.
Trek Diagnostic Systems is recalling VersaTREK Windows Software Version 5.4.3 because positive test results may incorrectly revert to negative in the database.
Biomet 3i is recalling Low Profile Abutments because some packages labeled as Hexed Castable Cylinders may contain Non-Hexed Castable Cylinders.