Mislabeling recalls
24 recalls.
- ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg recall (Prodose, Inc.)
DrugClass IIIReported November 4, 2026 · Incorrect label placed on product: Outer carton label correctly identifies drug product in bottle as ValuHealth Extra Strength Pain Relief Acetaminophen 500... - Evexias Health Solutions Amino Ultra recall (EVEXIAS HEALTH SOLUTION)
FoodClass IIReported October 28, 2026 · The product is mislabeled and fails to declare fish oil. - Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis recall (W L Gore & Associates, Inc.)
Medical deviceClass IIReported October 21, 2026 · The potential for the devices to be mislabeled with the incorrect length. - REF: P65 ST862 CoLag SCREW recall (In2bones USA, LLC)
Medical deviceClass IIReported October 21, 2026 · Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws. - Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter. - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Blom-Singer Classic Indwelling Voice Prosthesis recall (Freudenberg Medical, LLC)
Medical deviceClass IIReported August 12, 2026 · Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large... - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Pipeline Flex Embolization Device with Shield Technology recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20... - Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028 recall (Omnicell, Inc.)
Medical deviceClass IReported May 20, 2026 · Potential for mislabeled syringe produced by the i.v.STATION device. - french broad CHOCOLATE bette's bake sale recall (French Broad Chocolate Factory)
FoodClass IReported May 13, 2026 · Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor... - Label is predominantly green with white lettering in a clear plastic clamshell... recall (PURE PALM C/O DVD)
FoodClass IIReported April 22, 2026 · mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites) - XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm recall (XTANT Medical Holdings, Inc)
Medical deviceClass IIReported April 15, 2026 · Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is. - MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE recall (KOB GmbH)
Medical deviceClass IIReported March 18, 2026 · Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine. - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - Brand Name: Reverse Shoulder Prosthesis recall (Encore Medical, LP)
Medical deviceClass IIReported March 4, 2026 · Knee and Humeral socket implants contain incorrect labeling. - The Tuna Salad product container is mislabeled with a Chicken Salad lid recall (Reser's Fine Foods, Inc.)
FoodClass IReported February 25, 2026 · Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad. - Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported February 25, 2026 · Products were mislabeled as the 6mm product but included the 5 mm product. - spicely ORGANIC sumac NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled - spicely ORGANIC celery salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled - spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO... recall (Organic Spices, Inc)
FoodClass IIReported February 11, 2026 · Product contains salt and is mislabeled - BD Ready-to-Use Hydrophilic Catheter 14 Fr recall (HANGZHOU BEVER MEDICAL DEVICES CO., LTD.)
Medical deviceClass IIReported January 21, 2026 · Labeling error, Incorrect expiration date - BIOSURE HA SCREW recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported December 24, 2025 · Removal of affected lot of screws due to labeling error.