Safety Recalls
RSS ↗17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,151–2,200 of 17,553
- 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.
- Unclassified
Vehicle Recall · April 30, 2026
2025 GRAND DESIGN LINEAGEA detached solar panel can become a road hazard for other vehicles, increasing the risk of a crash.
- Unclassified
Consumer Product Recall · April 30, 2026
Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea
Earthtec 7 3/8 Inch Pool Drain CoversThe recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.
- Unclassified
Consumer Product Recall · April 30, 2026
Shenzhen Maikeer Industrial Co., Ltd., doing business as MalkerDirect, of China
Malker 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
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
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.
- 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
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320Lidocaine 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
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.U1; 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. SAMMC ANGIOGRAPHY SAMM066-15Affected 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, 3.0 mm, Extendable, Model/Catalog Number: 30.000.SEE.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
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320Lidocaine 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: 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
Halyard, Drape Pack. Kit Code: LMDP36-01.Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- Class II
Medical Device Recall · April 30, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225),It 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 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
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
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).
- 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
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
BD Pyxis Mini Main REF: 349 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- Class II
Medical Device Recall · April 30, 2026
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; 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
5# Sunflower Seeds C/NSThe 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 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 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 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
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
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.
- Unclassified
Vehicle Recall · April 29, 2026
2024 ROADTREK ZION SLUMBERA pop-top that lifts during transit can distract the driver, or detach if the secondary safety straps fail, increasing the risk of a crash.
- 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
Medical Device Recall · April 29, 2026
Beckman Coulter Biomedical GmbH
REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connectionsDue 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 in incorrect reporting of test outcomes.
- 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
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 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 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 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 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 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
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, 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 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 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 I
Food Recall · April 28, 2026
2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.Potential presence of Salmonella.
- Class I
Food Recall · April 28, 2026
MA Cohen's Kippered Herring vacuum packed, weight provided at retail, UPC 7232577992Clostridium botulinum is an uncontrolled hazard
- Class II
Medical Device Recall · April 28, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079,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.
- Class II
Medical Device Recall · April 28, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044The 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.
- Unclassified
Vehicle Recall · April 28, 2026
2024 FORD BRONCOA seat with a dislodged bolt may not properly restrain an occupant in a crash, increasing the risk of injury.
- Unclassified
Vehicle Recall · April 28, 2026
2024 HARLEY-DAVIDSON FLHX, 2024 HARLEY-DAVIDSON FLTRX, 2025 HARLEY-DAVIDSON FLHX, 2025 HARLEY-DAVIDSON FLTRX, 2026 HARLEY-DAVIDSON FLHX, 2026 HARLEY-DAVIDSON FLHXL, 2026 HARLEY-DAVIDSON FLTRXWhen the dipstick is removed while the crankcase is pressurized, oil may eject from the fill spout, increasing the risk of injury.
- 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.