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.
H E B is recalling Houston Culinary Center Greek Pasta Salad Kits sold in Texas due to the use of an ingredient with violative pesticide residue.
H E B is recalling 39 units of Yellowfin Tuna Salad Sandwiches in Texas due to violative pesticide residue.
H E B is recalling 182 units of 12-inch Artichoke Chicken Pizza sold in Texas due to violative pesticide residue.
H E B is recalling Herb Seared Salmon sold in Texas due to violative pesticide residue.
H E B is recalling HCC Salad Tuna Classic Yellowfin SS in Texas due to violative pesticide residue.
Bellisio Foods is recalling Boston Market boneless pork rib frozen entrees due to possible glass or hard plastic contamination. No injuries have been reported.
McNeilus is recalling 2015 Atlantic front loader trucks equipped with optional CNG tailgates because they may lack required rear and side rear red reflectors.
In2Bones is recalling 20 units of Model S25 ST014 osteosynthesis screws distributed in Tennessee because they were manufactured with the incorrect Torx imprint on the screw head.
RemedyRepack, Inc. is recalling 65 vials of Humulin 70/30 insulin due to incorrect storage instructions on the label.
Durrset Amigos Ltd. is recalling specific cans of Texas Style HEB Charro Beans because they may contain foreign material, including rocks.
Saputo Dairy Foods USA is recalling specific lots of chocolate whipped topping due to undeclared Red #40, Yellow #5, Yellow #6, and Blue #1 food colorings.
Pfizer is recalling Norpace CR (disopyramide phosphate) capsules because they failed to meet dissolution specifications. The recall covers specific lots distributed nationwide.
LeMaitre Vascular is recalling 4,315 units of NovaSil Silicone Embolectomy Catheters due to a manufacturing issue that may compromise sterility.
RemedyRepack Inc. is recalling Ascorbic Acid 500 MG/ML Injection vials because they contain incorrect storage instructions on the label.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters due to a manufacturing issue that may compromise sterility.
BioHorizons is recalling 32 units of 5.0 x 15mm dental implants because the packaging incorrectly listed the length as 10.5mm.
LeMaitre Vascular is recalling NovaSil Embolectomy Catheters due to a manufacturing issue that could compromise packaging sterility.
LeMaitre Vascular is recalling 4,315 Over-the-Wire Embolectomy Catheters worldwide due to a manufacturing defect that may compromise sterility.
Edwards Lifesciences is recalling Thin-Flex Venous Cannulas because the product guide incorrectly lists the connector size as 3/8 inch instead of the actual 1/2 inch.
Durrset Amigos Ltd. is recalling Texas Style HEB Charro Beans Spicy in 15 oz cans because they may contain foreign material, specifically rocks.
Valeant Pharmaceuticals is recalling 61 units of the SPAG-2 6000 aerosol generator because they were released without required particle size testing.
Powers Medical Devices is recalling 128 Pacifier Activated Lullaby (PAL) Systems because the units' labeling is inconsistent with their FDA-cleared indications.
Smith & Nephew is recalling 9 units of PERI-LOC Volar Distal Radius Plates that were laser marked and packaged with incorrect anatomical orientation.
Smith & Nephew is recalling 9 units of PERI-LOC VOLAR DISTAL RADIUS PLATES because they were laser marked and packaged with incorrect anatomical orientation.
Windstone Medical Packaging is recalling 40 kits of the AMS 4674 Custom Pack because they contain a recalled Seldinger Needle component.