Recall archive
32,364 recalls · page 16 of 1349
Reported Sep 30, 2026Updated Oct 7, 2026
Fi Calming Daily Supplement powder Net Weight 180g (6.35 oz) UPC: 8 50064 80011 1. Intended for use in dogs.
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Barking Labs Corp.
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
VITEK 2 AST-N461 TEST KIT, GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED, Reference Number 424811
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Red Blood Cells, Leukocytes Reduced
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Blood Assurance Inc.
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Red Blood Cells, Leukocytes Reduced
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Carter BloodCare
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 15, 2026
INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperVision, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Cornea
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CorneaGen - Boston
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Criticare Technologies, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Red Blood Cells
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Department
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 7, 2026
Whole Blood
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Department
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Pecorino Toscano D.O.P. STAGIONATO cheese wheels. Product of Italy. Each cheese wheel is approximately 3-4 lbs. Wheels…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elegant Foods, LLC
FDA (openFDA food enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Evergreen Fresh Sprouts LLC, Broccoli Sprouts, packaged in clear plastic zip lock bag, net wt. 4oz, UPC 8 38796 00105…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Evergreen Fresh Sprouts LLC
FDA (openFDA food enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Cornea
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eversight Illinois
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 7, 2026
Cornea
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eversight
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors; Model Number: 03-2522-1;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gias Food Inc.
FDA (openFDA food enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
GreenTripe.com Frozen Dog Food Xkaliber Net Wt. 1 lbs (453g). Packaged in rolls, 36 rolls per case. GreenTripe.com…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.GreenTripe.com,Inc.
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 7, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HCSC-Blood Center
2 more products in this recall
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module Model/Catalog Number: S3610, S2610,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heidelberg Engineering GmbH
FDA (openFDA device enforcement)
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