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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
June 26, 2025Electronics & BatteriesCPSC
DR Power Recalls Lithium-Ion Battery Packs Due to Fire and Burn Hazards
Hazard: The recalled battery packs can short-circuit and ignite, posing fire and burn hazards to consumers.
June 26, 2025OtherCPSC
iHerb Recalls Bottles and Blister Packs of California Gold Nutrition Iron Supplements Due to Risk of Serious Injury or Death from Child Poisoning; Violation of Federal Standard for Child Resistant Packaging
Hazard: The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The iron-containing dietary supplement packages violate the federal standard for child-resistant packaging because the bottles and blister packs are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.
June 26, 2025OtherCPSC
The Coleman Company Recalls Converta Camping Cots and Converta Camping Suspension Stretchers Due to Laceration and Amputation Hazards; Imported by Newell Brands
Hazard: The backrest fold mechanism can pinch consumers' fingers, posing laceration and amputation hazards.
June 25, 2025Medical DevicesFDA
Diagnostica Stago, Inc. recalls STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent
Hazard: Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1%
June 25, 2025Medical DevicesFDA
Fresenius Medical Care Holdings, Inc. recalls 5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline,
Hazard: Potential of blood leak occurring between the lower port of the venous chamber and the tubing include: hemodiafiltration (HDF), hemodialysis (HD), hemofiltration (HF), and isolated ultrafiltration.
June 25, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Plum Solos, Item number 400011001; infusion pump
Hazard: Internal testing found that Plum Duo pumps with software version 1.1.1 have a workflow that may result in bypassing the Maximum Dose Limit alert. The Maximum Dose Limit is set in the LifeShield Drug Library Manager (DLM) within the LifeShield Medication Management Safety Software and specifies the highest dose at which the pump can be programmed for weight or BSA (body surface area) based medication rulesets. The limit can be configured for Dose, Loading Dose, and Bolus Dose.
June 25, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
Hazard: Internal testing found that Plum Duo pumps with software version 1.1.1 have a workflow that may result in bypassing the Maximum Dose Limit alert. The Maximum Dose Limit is set in the LifeShield Drug Library Manager (DLM) within the LifeShield Medication Management Safety Software and specifies the highest dose at which the pump can be programmed for weight or BSA (body surface area) based medication rulesets. The limit can be configured for Dose, Loading Dose, and Bolus Dose.
June 25, 2025Medical DevicesFDA
BALT USA, LLC recalls Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00
Hazard: Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.
June 25, 2025Medical DevicesFDA
BALT USA, LLC recalls Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 0081006856885
Hazard: Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.
June 25, 2025Medical DevicesFDA
Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used i
Hazard: Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.
June 25, 2025Medical DevicesFDA
Chamberlain Technologies LLC recalls SURGIMESH WN, Polymeric Surgical Mesh, 14cm x 15cm Flat Sheet, Model/Catalog Number: T1415
Hazard: Potential presence of residual adhesive material on the mesh surface.
June 25, 2025Medical DevicesFDA
Chamberlain Technologies LLC recalls SURGIMESH XB, Polymeric Surgical Mesh, X-Large Ellipse Barrier Mesh, Model/Catalog Number: Tintra E-3030
Hazard: Potential presence of residual adhesive material on the mesh surface.
June 25, 2025Medical DevicesFDA
Chamberlain Technologies LLC recalls SURGIMESH XB, Polymeric Surgical Mesh, 14m x 15cm Flat Sheet with Silicone Barrier, Model/Catalog Number: Tintra R-1415
Hazard: Potential presence of residual adhesive material on the mesh surface.
June 25, 2025Medical DevicesFDA
Chamberlain Technologies LLC recalls SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Hazard: Potential presence of residual adhesive material on the mesh surface.
June 25, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia Max. Model Number: 10762473
Hazard: A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
June 25, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls UROSKOP Omnia. Model Number: 10094910
Hazard: A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
June 25, 2025Medical DevicesFDA
Ohio Medical Corporation recalls GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S
Hazard: Erroneous calibration values, potentially resulting in: as the device ages, oxygen purity will gradually decrease to the point where the device alarms to indicate low oxygen purity will be incorrect.
June 25, 2025Medical DevicesFDA
Guangzhou Pluslife Biotech Co., Ltd. recalls Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Catalog Number: RM101020
Hazard: Devices were distributed in the U.S. market without obtaining the required FDA premarket authorization (e.g., 510(k) clearance or PMA).
June 25, 2025Medical DevicesFDA
Guangzhou Pluslife Biotech Co., Ltd. recalls Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM001 Software Versio
Hazard: Devices were distributed in the U.S. market without obtaining the required FDA premarket authorization (e.g., 510(k) clearance or PMA).
June 25, 2025Medical DevicesFDA
Orthofix Srl recalls REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
Hazard: Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
June 25, 2025Medical DevicesFDA
HANGZHOU ACOSOUND TECHNOLOGY CO., LTD. recalls AcoSound. Model Number: LW12-BTE-M
Hazard: Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer's name is mislabeled as "Developed by AcoSound," Correct should be "Manufactured by Hangzhou AcoSound." And the labeling has no statement of the place of business for the manufacturer. 2. Customer information: The customer "Blaid" information is not correctly marked; Blaid is not the manufacturer. 3. UDI Information: The UDI information is incomplete and without DI information and correct Pl information, not complied with UDI label requirements.
June 25, 2025Medical DevicesFDA
Dexcom, Inc. recalls Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1),
Hazard: Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A missed audible alert for low or high blood glucose values could lead to untreated hypo or hyperglycemia which can cause seizures, vomiting, loss of consciousness, or death.
June 25, 2025Medical DevicesFDA
Dexcom, Inc. recalls Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-
Hazard: Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A missed audible alert for low or high blood glucose values could lead to untreated hypo or hyperglycemia which can cause seizures, vomiting, loss of consciousness, or death.
June 25, 2025Medical DevicesFDA
Dexcom, Inc. recalls Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 (MT26403-0), STK-AT-013 (MT26403-0),
Hazard: Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A missed audible alert for low or high blood glucose values could lead to untreated hypo or hyperglycemia which can cause seizures, vomiting, loss of consciousness, or death.
June 25, 2025Medical DevicesFDA
Dexcom, Inc. recalls Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
Hazard: Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A missed audible alert for low or high blood glucose values could lead to untreated hypo or hyperglycemia which can cause seizures, vomiting, loss of consciousness, or death.
June 25, 2025Medical DevicesFDA
Spectral Instruments Inc recalls Ami HTX.
Hazard: The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.
June 25, 2025Medical DevicesFDA
Spectral Instruments Inc recalls Lago X
Hazard: The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.
June 25, 2025Medical DevicesFDA
Cook Incorporated recalls Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are
Hazard: Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.
June 25, 2025Food & BeverageFDA
Bakkavor Foods USA, Inc. recalls CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen, In
Hazard: Foreign Object - Wood. The firm was notified by their supplier that the product may contain pieces of wood.
June 25, 2025Food & BeverageFDA
RGB Soda, LLC. recalls Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg. Th
Hazard: Potential contamination with Salmonella.