Recalls in April 2026
673 recalls.
- Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - Addall XR Shot 1 single bottle recall (ZMB Enterprises)
FoodClass IReported September 2, 2026 · The product contains 1,4-DMAA, Phenylethylamine and Phenibut. - navify Digital Pathology recall (Ventana Medical Systems, Inc.)
Medical deviceClass IIReported August 19, 2026 · Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window - BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL ... recall (MICROVENTION INC.)
Medical deviceClass IIReported August 19, 2026 · Due to an increase rate of balloon pinhole defects. - REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand... recall (Beckman Coulter Biomedical GmbH)
Medical deviceClass IIReported August 12, 2026 · Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog... recall (Prismatik Dentalcraft, Inc.)
Medical deviceClass IIReported July 29, 2026 · Due to device not having FDA Clearance - The intended use is to be paired with a weapon for aiming purposes. recall (Wilcox Industries Corp.)
Medical deviceClass IIReported July 29, 2026 · Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all... - Winfield's CWB Chocolate Bar recall (Chocolate Bar Holdings LLC)
FoodClass IIReported July 22, 2026 · Undeclared milk allergen. - Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator ... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote... recall (Elekta, Inc.)
Medical deviceClass IIReported July 15, 2026 · Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient. - Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported July 15, 2026 · Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if... - Revitaderm Wound Care recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated - Fungal Fusion ERADICATION Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - vite20 Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TERPENICOL Antifungal Cream recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIPENICOL S Antifungal Solution recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry - TRIFLUENT PHARMA TRIDERGEL Wound Care Gel recall (Blaine Labs Inc)
DrugClass IIReported July 8, 2026 · CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated - Revitaderm Wound Care Gel recall (Blaine Labs Inc)
DrugClass IReported July 8, 2026 · Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp - Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 ... recall (Covidien LLC)
Medical deviceClass IIReported July 8, 2026 · Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP. - Adapter for Head Positioning recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported July 8, 2026 · The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of... - Short Monobloc Stem Broaches recall (Medacta Usa Inc)
Medical deviceClass IIReported July 8, 2026 · Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the... - SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 ... recall (Mentor Texas LP)
Medical deviceClass IIReported July 8, 2026 · A single lot of expired syringes were distributed due to a distribution system control failure. - 25# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/NS recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 8/9.5oz Tub Nut - Sunflower Seed recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz No Salt Sunflower Seeds recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz Sunflower Seeds Salted recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 2.0 oz Dirty Sour Cream and Onion Potato Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.0 oz Dirty Maui Onion Chip recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - Joy Saffron Cardamon Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Orange Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Peach Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Mint Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Masala Chaash Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Plain Chaash Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Mango-Pina-Orange Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Mango-Pina-Strawberry Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Strawberry Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Pineapple Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Salty Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Sweet Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Rose Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Joy Mango Lassi 16 oz. recall (Joy Gourmet Foods LLC.)
FoodClass IIReported July 1, 2026 · Product not adequately pasteurized - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - INZONE DETACHMENT SYSTEM recall (Stryker Neurovascular)
Medical deviceClass IIReported July 1, 2026 · Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and... - Multi-Snare Set: 5 mm x 125 cm recall (PFM MEDICAL INC.)
Medical deviceClass IIReported July 1, 2026 · A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility... - Da Vinci ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported July 1, 2026 · Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would... - Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)
Medical deviceClass IIReported June 24, 2026 · Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses. - directCHECK ACT-LR whole blood quality control recall (Accriva Diagnostics, Inc.)
Medical deviceClass IIReported June 24, 2026 · Assayed Whole blood control contains labeling with incorrect performance range. - Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: PORT A CATH DYNJ906818A recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DAVINCI MAIN DYNJ908031D recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: WT LAVH PACK DYNJ46609F recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for...