Recalls in February 2026
364 recalls.
- PRIMAL HERBS recall (PRIMAL SUPPLEMENTS GROUP LLC)
FoodClass IReported October 28, 2026 · FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS recall (Encore Medical, LP)
Medical deviceClass IIReported July 15, 2026 · Due to packaging discrepancy with incorrect product size mixed up. - Radius VSM Disposable NIBP Cuff recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Radius VSM ECG pre-connected Set recall (Masimo Corporation)
Medical deviceClass IIReported July 8, 2026 · Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on... - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. KIT... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - TMJ Bilateral Implants recall (TMJ Solutions Inc)
Medical deviceClass IIReported July 1, 2026 · Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided... - WeiKFiELD Custard Powder Kesar Pista recall (Weikfield Foods Pvt. Ltd.)
FoodClass IIIReported June 17, 2026 · The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio. - The Large Volume Pump recall (Fresenius Kabi USA, LLC)
Medical deviceClass IIReported June 10, 2026 · Potential for the Cassette Loading Lever to break. - On-X Mitral Heart Valve with Conform-X Sewing Ring recall (On-X Life Technologies, Inc.)
Medical deviceClass IIReported May 20, 2026 · Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications. - XZL recall (SUNGAL INC)
FoodClass IIReported May 13, 2026 · Product Contains undeclared FD&C Yellow #5 & #6 and Red #40 - KLG recall (Ganesha Enterprises LLC)
FoodClass IIReported May 6, 2026 · Undeclared food colorings (Yellow 6, Blue 1, and Yellow 5) and unapproved Acid Red 14. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Kits: 1) ARTHROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) HYSTEROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) GYN LAPAROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) LABOR PACK-22025208-LF recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) ARTHROGRAM TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) SYR CONTROL 8ML ROTATING recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) NEWBORN ADMISSION recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) GENERAL LAPAROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) ENT PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) HEART TRANSPLANT BIOPSY recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) PICC TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) MTS LEFT HEART KIT-CAROLINAS HOS recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) CATH LAB CDS recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) ANGIOGRAPHY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Namic Syringes: 1) SYR CNTRL 10ML RING W/ROT NB recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL... recall (Clariance-SAS)
Medical deviceClass IIReported April 22, 2026 · Due to a quality issue regarding the presence of burr on the finished cervical plate product. - React Health PHOENIX 5L Oxygen Concentrator recall (3B Medical, Inc.)
Medical deviceClass IIReported April 22, 2026 · Devices which did not meet internal quality specifications were inadvertently distributed. - Multi-parameter Command Module recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported April 15, 2026 · Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve... - See Luer Cap Set recall (Molded Products Inc)
Medical deviceClass IIReported April 15, 2026 · Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve... - 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 medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Control Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - NAMIC Angiographic Syringe recall (Medline Industries, LP)
Medical deviceClass IReported April 15, 2026 · Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result... - Imu-Tek Colostrum-5 Powder recall (Imu-Tek Animal Health, Incorporated)
FoodClass IIReported April 8, 2026 · Product is potentially under-processed. - Imu-Tek Colostrum-5 120 Capsules recall (Imu-Tek Animal Health, Incorporated)
FoodClass IIReported April 8, 2026 · Product is potentially under-processed. - MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS recall (Super World Trading Inc.)
FoodClass IIIReported April 8, 2026 · Products contain cyclamates (banned sweetener) - Divided Sunset Multi Collagen Peptides recall (TG FOODS INC)
FoodClass IIReported April 8, 2026 · The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH... - Cardinal Health Monoject Tuberculin Syringe recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported April 8, 2026 · The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes... - SIGNA Premier systems recall (GE Healthcare LLC)
Medical deviceClass IIReported April 8, 2026 · Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous... - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan.