Safety Recalls
RSS ↗15,062 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 551–600 of 15,062
- Class I
Food Recall · May 1, 2026
#007415 Fiery Hot, Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094.Products may be potentially contaminated with Salmonella.
- Class I
Food Recall · May 1, 2026
#007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094Products may be potentially contaminated with Salmonella.
- Class II
Food Recall · May 1, 2026
SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
- Class I
Food Recall · May 1, 2026
#009530 Ranch Seasoning, Net Wt: 50 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094.Products may be potentially contaminated with Salmonella.
- Class I
Food Recall · May 1, 2026
Popping Topping, Sour Cream & Onion Flavored Popcorn Seasoning, Net Wt: 1.6oz. UPC 0 31851-01001 6. Distributed By: Butler's Pantry, 1224 Clark St. Watertown, WI 53094.Products may be potentially contaminated with Salmonella.
- 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.
- 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
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
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
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
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
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 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: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 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
BD Pyxis Mini Main REF: 349 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- 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.
- 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
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
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, 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 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
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.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
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
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
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 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
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
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).
- 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.
- 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.
- 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
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
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 II
Medical Device Recall · April 30, 2026
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20Lidocaine 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 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.
- 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
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.
- 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, 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
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 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
BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinetFingerprint scanner may overheat to a temperature to cause 1st degree burn.
- 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
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.
- 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
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
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).