Safety Recalls
RSS ↗17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,101–2,150 of 17,553
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
- Class II
Medical Device Recall · April 30, 2026
Halyard, Towel Six Pack. Kit Code: AMTS70-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.U1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class I
Medical Device Recall · April 30, 2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic EaDue to incorrect shelf-life expiration date.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
BD Pyxis MedStation ES REF: 323 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2Assayed Whole blood control contains labeling with incorrect performance range.
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
BD Pyxis MedStation ES Tower REF: 352 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Class II
Medical Device Recall · April 30, 2026
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura XperIt was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.
- Unclassified
Vehicle Recall · April 30, 2026
2025 GRAND DESIGN LINEAGEA loose base may allow the seat to move during a crash, increasing the risk of injury.
- Class II
Medical Device Recall · April 30, 2026
Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.1Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may increase the risk of fracture in the medial region of the proximal humerus.
- Class II
Medical Device Recall · April 30, 2026
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: NoLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Unclassified
Consumer Product Recall · April 30, 2026
Acer America Corporation, of Irvine, California
Acer AES015 Two-Wheeled Folding Electric ScootersA loose screw can cause the front tube to fold down unexpectedly, posing a risk of injury from a fall hazard.
- Class II
Medical Device Recall · April 30, 2026
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Class II
Medical Device Recall · April 30, 2026
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selecteDue to an increase rate of balloon pinhole defects.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Unclassified
Consumer Product Recall · April 30, 2026
Build-A-Bear Workshop, Inc., of St Louis, Missouri
Build-A-Bear Workshop Heartwarming Hugs BearsThe zipper slider on the side pouch can detach, posing a risk of serious injury or death from choking hazard to children.
- Class II
Medical Device Recall · April 30, 2026
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
- Unclassified
Consumer Product Recall · April 30, 2026
UHOMEPRO 5-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · April 30, 2026
American Honda Motor Co. Inc, of Torrance, California
Model Year 2025-2026 CRF250R/RX/RWE and CRF450R/RX/RWE Off-Road MotorcyclesThe handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard.
- Unclassified
Consumer Product Recall · April 30, 2026
Ningbopingyao E-Commerce Ltd., dba DGIVOVO US, of China
DGIVOVO US Electric Pressure WashersThe recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
- Unclassified
Consumer Product Recall · April 30, 2026
Thermos L.L.C., of Schaumburg, Illinois
Thermos Stainless King 3000 and 3020 Food Jars and Thermos Sportsman 3010 Food & Beverage BottlesIf perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in serious impact injury and laceration hazards to the consumer.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Class II
Drug Recall · April 30, 2026
Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus, OH 43204. NDC: 64380-474-01Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
- Class II
Medical Device Recall · April 30, 2026
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Unclassified
Vehicle Recall · April 30, 2026
2023 NOVA BUS LFSAn overloaded control unit may shutdown, causing a loss of drive power and increasing the risk of a crash.
- Unclassified
Consumer Product Recall · April 30, 2026
CBC Group, Inc., of Phoenix, Arizona
Stephan Baby Boo Bunnie and Friends Children's ToysThe toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards.
- Class I
Medical Device Recall · April 30, 2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
- Unclassified
Consumer Product Recall · April 30, 2026
Mobility Source Medical Technology Co., Ltd. of China
Hepo Adult Portable Bed RailsThe recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails also do not meet structural stability or retention strap requirements, posing a fall hazard. The bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard. In addition, the bed rails do not bear the required hazard warning labels.
- Unclassified
Consumer Product Recall · April 30, 2026
Bayer HealthCare LLC, of Whippany, New Jersey
Travel Size Afrin® Original Nasal Spray 6 mL BottlesThe 6 mL nasal sprays contain an imidazoline, which must be in child-resistant packaging or meet the labeling requirements for non-complying packaging, as required by the Poison Prevention Packaging Act. The 6 mL nasal spray's packaging is not child-resistant nor bears the required labeling statement, posing a risk of serious injury or illness from poisoning, if the contents are swallowed by young children.
- Unclassified
Consumer Product Recall · April 30, 2026
Alliance Chemical, of Taylor, Texas
1-K Kerosene Heater Fluid Portable Fuel ContainersThe pre-filled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. In addition, the Children's Gasoline Burn Prevention Act requires all closures on portable kerosene fuel containers to be child-resistant. The container is not child-resistant, posing a risk of burn and poisoning to children.