Safety Recalls
RSS ↗15,062 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 601–650 of 15,062
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.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
BD Pyxis MedStation 4000 REF: 303 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
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
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 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, 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
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube KitLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- Class I
Food Recall · April 30, 2026
Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - EgyptSalmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
- 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).
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.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, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; 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
Residential Elevators, Inc., of Crawfordville, Florida
Residential Elevators StrikeLock Hoistway Door Locking DeviceThe elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death due to fall and injury hazards.
- Class II
Medical Device Recall · April 30, 2026
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Class II
Medical Device Recall · April 30, 2026
Halyard, Pain Pack. Kit Code: AMPK48-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 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
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20Lidocaine 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, 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
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.
- Class II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24Lidocaine 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", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;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
Xiamen Fanlu Technology Co., Ltd., doing business as Smfanlus, of China
Qumeney Bicycle Light SetsThe recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the bicycle lights do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Unclassified
Consumer Product Recall · April 30, 2026
SOFT INC., of Denver, Colorado
Segmart 4-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.
- 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
BD Pyxis MedBank Tower REF: 1145-00 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
Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320Lidocaine 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
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2Assayed Whole blood control contains labeling with incorrect performance range.
- 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.
- 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
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 I
Food Recall · April 29, 2026
8/9.5oz Tub Nut - Sunflower SeedThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class II
Medical Device Recall · April 29, 2026
Boston Scientific Neuromodulation Corporation
Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSKReusable electrodes may not meet expected performance levels.
- Class II
Medical Device Recall · April 29, 2026
Plum Solo Precision IV Pump, 40001-0401Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
- Class II
Drug Recall · April 29, 2026
Zydus Pharmaceuticals (USA) Inc
Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; aCGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
- Class I
Food Recall · April 29, 2026
6/11oz Sunflower Seeds SaltedThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class II
Medical Device Recall · April 29, 2026
Plum Duo Precision IV Pump, 40002-0403Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
- Class II
Drug Recall · April 29, 2026
Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-099-03CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
- Class II
Drug Recall · April 29, 2026
Duloxetine Delayed-Release Capsules, 20 mg, Rx Only, 60 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-097-06.CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
- Class II
Drug Recall · April 29, 2026
Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC 27241-098-03, c) 1000 Capsules, NDC 27241-098-10, Marketed by: Ajanta Pharma USA Inc., BridgeCGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
- Class II
Medical Device Recall · April 29, 2026
Boston Scientific Neuromodulation Corporation
Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL,Reusable electrodes may not meet expected performance levels.
- Class II
Medical Device Recall · April 29, 2026
Plum Duo Infusion Pump, 40002-0401Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
- Class I
Food Recall · April 29, 2026
25# Sunflower Seeds C/SThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class I
Food Recall · April 29, 2026
6/11oz No Salt Sunflower SeedsThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class II
Drug Recall · April 29, 2026
Zydus Pharmaceuticals (USA) Inc
Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; (CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
- Class II
Medical Device Recall · April 29, 2026
Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with CurvThe Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
- Class I
Food Recall · April 29, 2026
5# Sunflower Seeds C/SThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class II
Medical Device Recall · April 29, 2026
Boston Scientific Neuromodulation Corporation
Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180Sterile anchors my lack sterility assurance.
- Class I
Food Recall · April 29, 2026
5# Sunflower Seeds C/NSThe firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
- Class II
Medical Device Recall · April 28, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027),The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
- Class II
Medical Device Recall · April 28, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 7222Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.