Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,001–3,050 of 15,186
- Unclassified
Consumer Product Recall · December 5, 2025
Shenzhen Topstar Industry Co., Ltd., of China
INIU BI-B41 Power BanksThe lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
- Class II
Food Recall · December 5, 2025
Eggs Potatoes Cheese Tacos, Evergreen Refreshments brand, Ready to Eat, Refrigerated. Net wt. 6.3 oz. UPC 100040103898, EG03698v01. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.Foreign material.
- Class II
Food Recall · December 5, 2025
Spicy Veggie Breakfast Burrito, Fresh to You, Ready to Eat, Refrigerated. Net wt. 9.1oz. UPC 100000010310, LPK110310V06. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057Foreign material.
- Class II
Medical Device Recall · December 5, 2025
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23Incorrect expiration date
- Class II
Food Recall · December 5, 2025
SOMA KITCHEN NATURAL ASAFOETIDA Net Wt. 4 oz (0.25 lb) Product of India Manufactured for and Imported by: Bharat Bazar, Fremont, CA 94539 Use by : JULY-2027 Lot : NATL/ASFTP/G/24 (BB/ASFTP/G/24) UPC :Undeclared wheat.
- Class II
Food Recall · December 5, 2025
Spicy Breakfast Burrito, Sprig & Sprout brand, Ready to Eat. Refrigerated. Net wt. 9.1oz. UPC 100001000297, SS00297v02. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.Foreign material.
- Class II
Food Recall · December 5, 2025
Spicy Egg Potatoes Cheese Tacos, Fresh to You brand, Ready to Eat, Refrigerated. Net wt. 6.3oz. UPC 100000010389, LPK110369V06. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.Foreign material.
- Class II
Medical Device Recall · December 5, 2025
Beaver-Visitec International, Inc.
BVI Leos Laser and Endoscopy System. Model Number: OME6000U.Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The omission of the ferrites on the USB communication cable results in non-conformance to the design specifications, which require two ferrites (one at each end of the cable).
- Class II
Medical Device Recall · December 4, 2025
Allwell Inflation Device, for angiographic use REF: IS-30-AInflation device handle may detach from the syringe during procedure.
- Class II
Medical Device Recall · December 4, 2025
Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
- Class II
Food Recall · December 4, 2025
Grandma Belle's Tomato Basil Soup, Net Wt. 17 oz. (482g), packaged in a glass jar, UPC 810084612293, Made By: Lil' Turtles 504 North Ray Street, Baltic, Ohio 43804, packed 12 jars per caseUndeclared allergen - milk
- Class II
Medical Device Recall · December 4, 2025
Impella 5.5 with SmartAssist¿ S2, Impella 5.5 with SmartAssist S2 Set, AU.Device packaged in incorrect outer box carton.
- Class II
Medical Device Recall · December 4, 2025
Allwell Angioplasty Pack REF: IS-30-B1/BInflation device handle may detach from the syringe during procedure.
- Class II
Medical Device Recall · December 4, 2025
Merit Medical , Custom Manifold Kit REF: K09-13203AInflation device handle may detach from the syringe during procedure.
- Unclassified
Consumer Product Recall · December 4, 2025
Jiangsu Liangjiang Intelligent Furniture Co., Ltd, of China
FUFU&GAGA White Wood Frame Queen Size Murphy Wall BedsDuring assembly or disassembly, the 215-pound frame of the wall bed can fall onto consumers, posing deadly impact, crush, and laceration hazards.
- Class II
Medical Device Recall · December 4, 2025
Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 AB9U14080090 AB9U12080090 AB9U14060090 AB9G14100090 AB9G1Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in stent migration.
- Class II
Food Recall · December 4, 2025
Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6elevated levels of chloramphenicol in frozen shrimp
- Class II
Medical Device Recall · December 4, 2025
Merit Medical , Custom Waste Management Kit Vascular Tray REF: K10T-05261Inflation device handle may detach from the syringe during procedure.
- Unclassified
Consumer Product Recall · December 4, 2025
Primark US Corp., of Boston, Massachusetts
Primark Water Balloon PumpThe water balloon pump can generate excessive pressure during use, causing the product to rupture, posing a risk of physical injury to the user or bystanders.
- Class II
Medical Device Recall · December 4, 2025
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version: N/A Product Description: The Ion Endoluminal System is a robotically assisted pDue to probe bags that may have a compromised or incomplete sterile pouch seal.
- Unclassified
Consumer Product Recall · December 4, 2025
Shenzhen Excellence Qichuang Technology, dba Vatos Toys, of China
Cubimana Treehouse Building Toy SetsThe building toy sets violate the mandatory safety standard because the battery compartment within the LED light piece contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Class I
Food Recall · December 4, 2025
Healthy Truth brand Moringa Powder; 5lb and 20lbProducts may be contaminated with Salmonella Richmond.
- Class II
Medical Device Recall · December 4, 2025
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H IN4130/JPH IN4130/K IN4130/KRK IN4130/L IN4130/T IN4230/JPH IN4230/K IN4330/CNK IN4330Inflation device handle may detach from the syringe during procedure.
- Class II
Medical Device Recall · December 4, 2025
Merit Medical , Custom Inflation Kit REF: K05-00761F K05-01717B K05-02080D K05-02090C K05-02221 K05-02338 K05-02470 K05-02954 K05-03094A K05T-00380C K05T-01674B K05T-01863 K05T-01915 K05T-01920F K05TInflation device handle may detach from the syringe during procedure.
- Class II
Medical Device Recall · December 4, 2025
Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
- Class II
Medical Device Recall · December 4, 2025
Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A K12T-07956 K12T-10922BInflation device handle may detach from the syringe during procedure.
- Unclassified
Consumer Product Recall · December 4, 2025
Changzhou Municipal Sea Metal Products Co. Ltd., of China
Casaottima 13-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · December 4, 2025
CreateOn, LLC, of Wheeling, Illinois
CreateOn Crayola-branded pip-CubesThe recalled magnetic building cubes contain magnets that can become loose if the seams separate, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- Unclassified
Consumer Product Recall · December 4, 2025
Grizzly Industrial Inc., of Bellingham, Washington
G0815 15" 3HP Heavy-Duty PlanersThe chip breaker can contact the cutterhead blades during use, which can cause debris to be ejected from the planer, posing impact and laceration hazards to the user and bystander.
- Unclassified
Consumer Product Recall · December 4, 2025
HydroJug, Inc., of Ogden, Utah
14-ounce Children's Sport TumblerThe rivets on the handle can come loose, causing the handle to detach, posing a choking hazard for children.
- Unclassified
Consumer Product Recall · December 4, 2025
Banghe Guangzhou International Trade Co., Ltd., dba KTEBO, of China
KTEBO Writing Tablet ToyThe recalled toys violate the mandatory standard for toys because the screw used to secure the battery compartment that contains a button cell battery does not remain attached as required. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Unclassified
Consumer Product Recall · December 4, 2025
Little Pea Shop Crib BumpersThe recalled crib bumpers violate the federal crib bumper ban because they can obstruct an infant's breathing, posing a risk of serious injury or death, due to suffocation. This creates an unsafe sleeping environment for infants. Padded crib bumpers are banned by the Safe Sleep for Babies Act.
- Class II
Medical Device Recall · December 3, 2025
SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Medical Device Recall · December 3, 2025
Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Unclassified
Vehicle Recall · December 3, 2025
2025 BMW X3A loss of rear brake function increases the risk of a crash.
- Class II
Medical Device Recall · December 3, 2025
Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Food Recall · December 3, 2025
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag per case. Net wt. 30 lbs. UPC 1 00 72714 00215 8. McCain Foodservice Solutions.Clear hard plastic fragments.
- Class II
Medical Device Recall · December 3, 2025
Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF H74939186251210; 2) 3.5mm x120mm, 150 cm, UPM/Model No. REF H74939186351210;Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter devices due to the potential for inflation/deflation difficulty during use in the peripheral vasculature. An internal investigation found that a manufacturing process variation resulted in catheters that may not properly inflate/deflate. This was limited to Coyote OTW batches manufactured from 12Sep2025 through 13Oct2025. The processing variation has since been addressed. No other material numbers or batches are impacted by this removal.
- Class II
Medical Device Recall · December 3, 2025
Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Medical Device Recall · December 3, 2025
Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Medical Device Recall · December 3, 2025
Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class I
Food Recall · December 3, 2025
Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC 0 18169-66862 7. Lunds & Byerlys, Edina, MN 55424Undeclared allergens (Peanut, Egg, Soy)
- Class II
Food Recall · December 3, 2025
Sysco Imperial Potato Tater Barrel, item number 1000006067. Frozen potato product is packaged in 6/5 lb. clear unlabeled poly bags per case. UPC 1 07 34730 62740 0. Distributed by Sysco Corporation,Clear hard plastic fragments.
- Class III
Food Recall · December 3, 2025
1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643846, Distributed by Bendon, Inc. 2) Mickey Mouse Heart-ShapUnapproved color additive - chlorophyllin copper complex
- Class II
Medical Device Recall · December 3, 2025
Philips Healthcare (Suzhou) Co., Ltd.
Philips Incisive CTPotential for incomplete scan due to unstable connection inside of floating sensor.
- Class II
Medical Device Recall · December 3, 2025
BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03, 139676-01, 139421-01, 139420-01, 139419-01, 139419-02, 139673-01, 137081-01, 136Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
- Class II
Medical Device Recall · December 3, 2025
Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Medical Device Recall · December 3, 2025
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
- Class II
Medical Device Recall · December 3, 2025
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
- Class II
Medical Device Recall · December 3, 2025
Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).