Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,601 - 2,625 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0720 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1288-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm; Material Number (UPN): M00553520; Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is prolongation of the procedure to exchange the device for a new one. The most serious reasonably foreseeable outcome in cases where the first flange is unable to deploy or expand would be a cascade of events resulting in additional intervention, either endoscopic or surgical, to remove the stent and close the puncture site.	FDA Z-1161-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 19, 2025	Details
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-431Q-0720 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1270-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number: 81557 Software Version: Not Applicable Product Description: Lumipulse G pTau 217 Plasma Calibrators: The pTau 217 plasma concentration of a specimen is automatically calculated from the calibration curve, which is also automatically calculated from calibration data. The result of the calculation is reported in pg/mL. Lumipulse G pTau 217 Plasma Calibrators: Liquid (Frozen), 1x1.5 mL (5 Concentrations) CAL 1 0 pg/mL pTau 217 Plasma Calibrator CAL 2 0.250 pg/mL pTau 217 Plasma Calibrator CAL 3 1.000 pg/mL pTau 217 Plasma Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).	FDA Z-1303-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 11, 2025	Details
Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001; A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.	FDA Z-1308-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 17, 2025	Details
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1296-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0730 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1289-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Exploro Highly Sensitive Male Fertility / Sperm Concentration Test Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.	FDA Z-1263-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 22, 2025	Details
VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n) o Ceftazidime/avibactam (cza02n) o Meropenem/Vaborbactam (mev01n) o Imipenem (ipm05n) o Imipenem/Relebactam (ipr01n); CARD NAME/ PRODUCT REFERENCE: AST-N399 423701 AST-N402 423644 AST-N403 423645 AST-N404 423664 AST-N405 423864 AST-N406 423869 AST-N407 423870 AST-N409 423925 AST-N412 423936 AST-N413 423928 AST-N414 423933 AST-N415 423934 AST-N416 423935 AST-N417 423880 AST-N419 423948 AST-N421 424055 AST-N428 424320 AST-N429 424321 AST-N430 424322 AST-N433 424389 AST-N439 424501 AST-N440 424502 AST-N443 424541 AST-N444 Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species and/or Pseudomonas aeruginosa with the identified antibiotic formulations. Issue may lead to QC failure or false resistant results.	FDA Z-1236-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 5, 2026	Details
Male Fertility Sperm Test for Home Use (Cassette) Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.	FDA Z-1262-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 22, 2025	Details
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0725; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1273-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0330; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1271-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mobile hoists) Model/Catalog Number: 1430116,1430117,1430115 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.	FDA Z-1311-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 17, 2025	Details
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Product Description: Lumipulse pTau 217 Plasma Controls: This quality control product can be used as an objective judgement of the laboratory s procedures and personnel techniques when analyzing pTau 217 in K2EDTA plasma on the LUMIPULSE G System. It is a valuable tool to assess good laboratory practices. Two levels of control are available to compare observations with expected ranges therefore assuring consistent performance of the testing system within the clinical range. Lumipulse p Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).	FDA Z-1304-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 11, 2025	Details
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1287-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1290-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conjunction with a cyanide-free lytic agent for counting and sizing blood cells on all UniCel DxH Coulter Cellular Analysis Systems. For use as a rinsing agent on the UniCel DxH Slidemaker Stainers. For use as a diluent in conjunction with DxH ECO Cell Lyse for counting and sizing blood cells. For use as a rinsing agent. Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.	FDA Z-1221-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 10, 2025	Details
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25GA Convenience Kit - XES VS0644.25-XES There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.	FDA Z-1249-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 16, 2025	Details
JUICE from the Raw, DETOX GREENS Under-processed product may contain pathogenic bacteria that could harm to humans.	FDA H-0450-2026	Food	High	Feb 11, 2026 Recall: Jul 24, 2025	Details
JUICE from the Raw, sweet greens Under-processed product may contain pathogenic bacteria that could harm to humans.	FDA H-0451-2026	Food	High	Feb 11, 2026 Recall: Jul 24, 2025	Details
BarbaCuban 455 Everything Sauce (Hot), Net Wt 12 oz (355 ml) 12 oz glass bottles, and 1 gallon HDPE Industrial Plastic Jugs, ¿ gallon HDPE Industrial Plastic Jugs. packaged in 12x12 fl oz, 6x12 fl oz, 4x1 gallon, 4x1/2 gallons. UPC code 7 19660 00083 0 Undeclared Quinine	FDA H-0445-2026	Food	High	Feb 11, 2026 Recall: Dec 17, 2025	Details
WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt. 17oz. UPC 0267279 807987. Product is Take & Bake and sold refrigerated in a plastic flexible film as a single retail unit with a 5 day Sell-By date. Distributed by WinCo Foods 650 N. Armstrong Pl. Boise, ID. Product may contain foreign material (metal fragments).	FDA H-0449-2026	Food	High	Feb 11, 2026 Recall: Jan 15, 2026	Details
spicely ORGANIC celery salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO PRESERVATIVES - NO WHEAT NO SUGAR - NO SALT - NO IRRADIATION Net wt: 2.4oz (68g) Ingredients: Salt, Celery Seeds Organic www.spicely.com Organic Spices Inc, Fremont CA 94538 UPC: 826998007605 Product contains salt and is mislabeled	FDA H-0464-2026	Food	High	Feb 11, 2026 Recall: Jan 14, 2026	Details
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Blue Spirulina and Raspberry- UPC# 5065006235813 potential Clostridium botulinum contamination	FDA H-0473-2026	Food	High	Feb 11, 2026 Recall: Jan 9, 2026	Details
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Mango and Pineapple- UPC# 5065006235301 potential Clostridium botulinum contamination	FDA H-0476-2026	Food	High	Feb 11, 2026 Recall: Jan 9, 2026	Details

Showing 2,601 - 2,625 of 3,083 product recalls

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Product Recalls Today

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Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

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Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

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