recall database
FDA Recalls
An FDA recall is a company- or FDA-initiated removal or correction of a drug or medical device already on the market because it is defective or could be a health risk. Argus HQ tracks 4,082 published recalls from 2026 to 2026, filterable by classification (Class I, II, or III), year, and product category, each sourced from and linked back to fda.gov.
- Sterling Pharmaceutical Services LLC — Class II recall: AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Dro…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Midmark Corporation — Class II recall: Midmark IQvitals Zone, automatically and noninvasively measures systolic and dia…
Midmark Corporation·Class II·Medical device·September 30, 2026
- Philips North America Llc — Class II recall: Achieva XR; Model Numbers (REF): 1. 781153, 2. 781253;
Philips North America Llc·Class II·Medical device·September 30, 2026
- Sterling Pharmaceutical Services LLC — Class II recall: AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Dro…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Sterling Pharmaceutical Services LLC — Class II recall: Walgreens Lubricant Eye Drops, 0.5 FL OZ (15 mL) 1.0 FL OZ (30 mL) TOTAL, 2 coun…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Philips North America Llc — Class II recall: MR 7700 and Upgrade to MR 7700; Model Number (REF): 1. 782120, 2. 782153, 3. 78…
Philips North America Llc·Class II·Medical device·September 30, 2026
- Philips North America Llc — Class II recall: Evolution upgrade 1.5T and Evolution upgrade 3.0T; Model Numbers (REF): 1. 7821…
Philips North America Llc·Class II·Medical device·September 30, 2026
- DeRoyal Industries Inc — Class II recall: REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
DeRoyal Industries Inc·Class II·Medical device·September 30, 2026
- CooperVision, Inc. — Class II recall: Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Mode…
CooperVision, Inc.·Class II·Medical device·September 30, 2026
- CooperSurgical, Inc. — Class I recall: INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tub…
CooperSurgical, Inc.·Class I — most serious·Medical device·September 30, 2026
- Becton, Dickinson and Company — Class II recall: ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927…
Becton, Dickinson and Company·Class II·Medical device·September 30, 2026
- Criticare Technologies, Inc. — Class II recall: nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E…
Criticare Technologies, Inc.·Class II·Medical device·September 30, 2026
- Olympus Corporation of the Americas — Class II recall: Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD…
Olympus Corporation of the Americas·Class II·Medical device·September 30, 2026
- Philips North America Llc — Class II recall: Ingenia 3.0T and Ingenia 3.0T CX; Model Numbers (REF): 1. 781342(3.0T), 2. 7813…
Philips North America Llc·Class II·Medical device·September 30, 2026
- Sterling Pharmaceutical Services LLC — Class II recall: Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%,…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Macleods Pharmaceuticals Limited — Class III recall: Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleo…
Macleods Pharmaceuticals Limited·Class III — least serious·Drug·September 30, 2026
- Boston Scientific Corporation — Class I recall: Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M0…
Boston Scientific Corporation·Class I — most serious·Medical device·September 30, 2026
- Sterling Pharmaceutical Services LLC — Class II recall: Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distr…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Olympus Corporation of the Americas — Class II recall: Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm. Model Num…
Olympus Corporation of the Americas·Class II·Medical device·September 30, 2026
- Olympus Corporation of the Americas — Class II recall: Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-…
Olympus Corporation of the Americas·Class II·Medical device·September 30, 2026
- Sterling Pharmaceutical Services LLC — Class II recall: Walgreens Lubricant Eye Drops, Carboxymethylcellulose sodium 0.5%, Lubricant Eye…
Sterling Pharmaceutical Services LLC·Class II·Drug·September 30, 2026
- Fresenius Medical Care Renal Therapies Group, LLC — Class II recall: CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer…
Fresenius Medical Care Renal Therapies Group, LLC·Class II·Medical device·September 30, 2026
- Biomerieux Inc — Class II recall: VITEK 2 AST-N461 TEST KIT, GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED, Ref…
Biomerieux Inc·Class II·Medical device·September 30, 2026
- Philips North America Llc — Class II recall: Achieva 3.0T; Model Numbers (REF): 1. 781177, 2. 781277, 3. 781278, 4. 781344,…
Philips North America Llc·Class II·Medical device·September 30, 2026
- Philips North America Llc — Class II recall: Ingenia Elition S and Ingenia Elition X; Model Numbers (REF): 1. 781357(S), 2.…
Philips North America Llc·Class II·Medical device·September 30, 2026