Recent FDA Class II device recalls
320 recent FDA Class II device recalls are listed from U.S. FDA openFDA, dated 2026-09-30 to 2026-10-28; the most frequent is ASP Global, LLC. with 64. Data last updated 2026-11-03; each record links to its official source and a full report.
Data as of · Compiled by Zalwin from U.S. FDA openFDA
Includes: Record, Specialty, Date, Review days, Recall class, official source URL and score · Card, Apple Pay, Google Pay or Link via Stripe
320 records from U.S. FDA openFDA, dated 2026-09-30 to 2026-10-28. Most frequent: ASP Global, LLC. (64). Each record links to a full report and the official source.
Last updated 2026-11-03. Source: U.S. FDA openFDA.
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- ASP Global, LLC. (64)
- Boston Scientific Cork, Ltd. (41)
- Medline Industries, LP (35)
- AVID Medical, Inc. (17)
- Philips North America (13)
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What are the top recent FDA Class II device recalls right now?
Browse 35 more matching record reports
- Class II recall Z-0260-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0267-2027: Medtronic Neuromodulation
- Class II recall Z-0194-2027: Medtronic Navigation, Inc.
- Class II recall Z-0227-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0237-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0259-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0233-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0278-2027: Medline Industries, LP
- Class II recall Z-0226-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0244-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0262-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0263-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0238-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0241-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0223-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0203-2027: Medtronic MiniMed, Inc.
- Class II recall Z-0225-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0277-2027: Medline Industries, LP
- Class II recall Z-0240-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0192-2027: Think Surgical, Inc.
- Class II recall Z-0247-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0234-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0193-2027: B Braun Medical Inc
- Class II recall Z-0228-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0198-2027: Axonics, Inc.
- Class II recall Z-0257-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0272-2027: Medline Industries, LP
- Class II recall Z-0199-2027: Philips North America
- Class II recall Z-0283-2027: AVID Medical, Inc.
- Class II recall Z-0256-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0280-2027: Medline Industries, LP
- Class II recall Z-0239-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0195-2027: Medtronic Navigation, Inc.
- Class II recall Z-0250-2027: Boston Scientific Cork, Ltd.
- Class II recall Z-0249-2027: Boston Scientific Cork, Ltd.
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510(k) clearances (414) Class I device recalls (19) Class III device recalls (11)
Browse by specialty
Radiology (56) Orthopedic (53) Cardiovascular (52) General & Plastic Surgery (44) Dental (32) Gastroenterology & Urology (27) Neurology (23) Microbiology (21) Clinical Chemistry (15) General Hospital (14) Anesthesiology (12) Obstetrics & Gynecology (9) Ophthalmic (7)
Browse by record type by specialty
Radiology devices: recent FDA 510(k) clearances (56) Orthopedic devices: recent FDA 510(k) clearances (53) Cardiovascular devices: recent FDA 510(k) clearances (52) General & Plastic Surgery devices: recent FDA 510(k) clearances (44) Dental devices: recent FDA 510(k) clearances (32) Gastroenterology & Urology devices: recent FDA 510(k) clearances (27) Neurology devices: recent FDA 510(k) clearances (23) Microbiology devices: recent FDA 510(k) clearances (21) Clinical Chemistry devices: recent FDA 510(k) clearances (15) General Hospital devices: recent FDA 510(k) clearances (14) Anesthesiology devices: recent FDA 510(k) clearances (12) Obstetrics & Gynecology devices: recent FDA 510(k) clearances (9) Ophthalmic devices: recent FDA 510(k) clearances (7)
Frequently asked questions
How many recent FDA Class II device recalls are listed?
320 records from U.S. FDA openFDA, last refreshed automatically. The most recent is dated 2026-10-28.
Can I get alerts for Class II device recalls?
Yes. FDAPulse can email you new records matching this filter; plans are listed on the FDAPulse page.
Source: U.S. FDA openFDA. Informational only. RSS feed of new records
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