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.
ProSupps USA LLC is recalling Mr. Hyde Fruit Punch supplements in the US and Canada because they contain the unapproved ingredient picamilon.
The Metrix Company is recalling Secure 100mL empty vinyl containers because the hot stamp label incorrectly states the material. The bags are correctly made of PVC.
Ricker Hill Farms is recalling specific apple cider products because they contain patulin levels exceeding FDA limits.
ProSupps USA LLC is recalling DNPX Powder, 30 Pineapple Punch, because it contains the unapproved ingredient picamilon.
The Binding Site Group is recalling 361 Human Alpha-1-Antitrypsin Kits because the high control may recover low and fall out of range.
ProSupps USA LLC is recalling Mr. Hyde and Hyde V2 supplements because they contain the unapproved ingredient picamilon.
Radiometer America is recalling AutoCheck5+ Level 2 quality control ampoules because they may provide incorrect pCO2 and pO2 results.
Vi-Jon, Inc. is recalling 348,384 bottles of Magnesium Citrate Oral Solution because the product failed impurities and degradation specifications.
Inopak Ltd is recalling Choice Antibacterial Hand Soap due to GMP deviations and potential bacterial contamination from a pump.
ProSupps USA LLC is recalling Dr. Jekyll 30 Watermelon and Dr. Jekyll Watermelon V2 supplements because they contain the unapproved ingredient picamilon.
ProSupps USA LLC is recalling 25,318 units of Mr. Hyde Green Apple domestic sample packs because they contain the unapproved ingredient picamilon.
ProSupps USA LLC is recalling 573 units of Vanish V3 because the product contains the unapproved ingredient picamilon. The affected units were distributed in the US and Canada.
Quickie Stores, Inc. is recalling New York Deli tempeh sandwiches due to undeclared wheat. The recall affects 50 packages sold in Washington.
ProSupps USA LLC is recalling Dr. Jekyll V2 Orange Burst supplements because they contain the unapproved ingredient picamilon.
ProSupps USA LLC is recalling Dr. Jekyll V2 Mango Passion Fruit dietary supplements because they contain the unapproved ingredient picamilon.
ProSupps USA LLC is recalling Hyde V2 Berry Blast because it contains the unapproved ingredient picamilon. The product was distributed in the US and Canada.
Quickie Stores, Inc. is recalling Smoked Tempeh sandwiches due to undeclared wheat. The recall affects 50 packages sold in Washington.
Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.
Carl Zeiss Meditec AG is recalling nine INTRABEAM PRS 500 radiation therapy devices because they had incorrect printed calibration values on their certificates.
ProSupps USA LLC is recalling Hyde V2 Watermelon supplements because they contain the unapproved ingredient picamilon. The products were distributed in the US and Canada.
ProSupps USA LLC is recalling Dr. Jekyll Green Apple V2 domestic because it contains the unapproved ingredient picamilon.
ProSupps USA LLC is recalling specific Mr. Hyde Blue Razz dietary supplements because they contain the unapproved ingredient picamilon.
Bomimed is recalling specific lots of Disposable Fiber Optic Medium Laryngoscope Handles due to a potential for intermittent lighting during use.
Inopak Ltd is recalling specific batches of Mild Healthcare Antibacterial Hand Soap due to potential bacterial contamination from a defective pump.
Ultradent Products is recalling sterile Paper Points because the barcode label was placed underneath the sterile barrier, compromising the product's sterility.