Recalls in February 2026 (page 2)
364 recalls.
- 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. - 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. - 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. - 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. - 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. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Paradigm REAL-Time Veo Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 530G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm REAL-Time Revel Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm REAL-Time Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - Paradigm Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 620G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 740G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 720G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 700G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 640G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 770G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 630G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MiniMed 670G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 8, 2026 · All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of... - MEDLINE ANTERIOR HIP PACK DYNJ64672B recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BAL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - THORACIC ROBOTS recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Airway Exam Kit recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - 2.4 VOLT recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Sterile Radiology Procedure Kits recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility. - Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT ... recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - ENFIT G-TUBE CONNECTOR recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 recall (Stryker Communications)
Medical deviceClass IIReported April 8, 2026 · Surgical light assembly may not adequate support the weight of the ceiling cover. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH ... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - BD Kiestra" ReadA recall (BD KIESTRA LAB AUTOMATION)
Medical deviceClass IIReported April 8, 2026 · In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported April 8, 2026 · A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate... - RefleXion X1 Radiotherapy System Model RXM1000 recall (Reflexion Medical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied... - Blue Ventilator Adapter Module recall (Baxter Healthcare Corporation)
Medical deviceClass IReported April 8, 2026 · Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported April 8, 2026 · Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5... - Purge Cassette recall (Abiomed, Inc.)
Medical deviceClass IReported April 8, 2026 · Increased risk of purge leaks with Generation 1 purge cassettes. - SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD recall (Savannah Bee Company Inc.)
FoodClass IIReported April 1, 2026 · Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the... - Pepsin 1:3000 Powder recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - Pepsin 1:10 recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - Pepsin Full Strength Powder recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - King Harvest brand Spinach Hummus. Product is packed in 10oz plastic tubs with a clear... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - King Harvest brand Black Olive Hummus. Product is packed in 10oz plastic tubs with a... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - King Harvest brand Balsamic Hummus. Product is packed in 10oz plastic tubs with a... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - King Harvest brand Sundried Tomato Hummus. Product is packed in 10oz plastic tubs with... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - King Harvest brand Roasted Red Pepper Hummus. Product is packed in 10 and 17 oz... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - King Harvest brand Jalapeno Hummus. Product is packed in 10 and 17 oz plastic tubs... recall (Pacific Coast Fresh CO)
FoodClass IIReported April 1, 2026 · Foreign material (aluminum pieces). - Sunflour Bakery Hamburger Bun recall (NRS Enterprises, Inc. dba Sunflour Bakery)
FoodClass IIReported April 1, 2026 · Undeclared sesame seed ingredient in hamburger buns. - Levothyroxine Sodium Tablets USP 150 mcg recall (MACLEODS PHARMA USA, INC)
DrugClass IIReported April 1, 2026 · Subpotent Drug - Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall (Radnostix)
DrugClass IIIReported April 1, 2026 · Failed Tablet/Capsule Specifications - Embrace Drill Tower recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported April 1, 2026 · The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the... - Embrace Drill Tower recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported April 1, 2026 · The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the... - Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING recall (Medline Industries, LP)
Medical deviceClass IIReported April 1, 2026 · Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound... - BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall (CareFusion 303, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus HALO PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PK Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name:... recall (AMO Puerto Rico Manufacturing, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as... - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Imactis CT-Navigation System recall (GE Medical Systems, LLC)
Medical deviceClass IIReported April 1, 2026 · There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position. - Handy Solutions Neck & Shoulders Heating Pad recall (Navajo Manufacturing Company)
Medical deviceClass IReported April 1, 2026 · If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad... - BioFlo DuraMax Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - DuraMax Chronic Hemodialysis Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - 16F Dual Valved Splittable Sheath Introducer recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - ProGuide Chronic Dialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - CentrosFLO Hemodialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg... recall (Shaman Botanicals, LLC)
FoodClass IReported March 25, 2026 · A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification. - Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg... recall (Shaman Botanicals, LLC)
FoodClass IReported March 25, 2026 · A sample of the product had the active ingredient in a quantity greater than the labeled specification. - Wawa Chocolate Low-fat Milk 16 oz recall (Wawa Beverage Company)
FoodClass IIReported March 25, 2026 · Foreign plastic material discovered on fill line. - Wawa Cookies & Cream Milk 16 oz recall (Wawa Beverage Company)
FoodClass IIReported March 25, 2026 · Foreign plastic material discovered on fill line. - Wawa Double Dutch Chocolate Milk recall (Wawa Beverage Company)
FoodClass IIReported March 25, 2026 · Foreign plastic material discovered on fill line. - Wawa Reduced Fat Milk 2% 16 oz recall (Wawa Beverage Company)
FoodClass IIReported March 25, 2026 · Foreign plastic material discovered on fill line.