FDA Medical Devices
All recall actions attributed to FDA Medical Devices in our federal database. Each record links back to the agency's official notice so you can verify status, remedy, and amendments before acting.
U.S. Food and Drug Administration — Medical device recalls
39,096 recalls · Page 526 of 782
FDA Medical Devices Recall Insight
PlainRecalls tracks 39,096 recall actions attributed to the FDA Medical Devices in our federal recall index. Across the full PlainRecalls database of 101,704 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 38.4% of all indexed recalls. The agency's stated scope - U.S. Food and Drug Administration — Medical device recalls - determines what classes of products flow through its recall pipeline and how quickly notices reach consumers. With 782 pages of records at 50 recalls per page, this archive represents one of the longest continuous federal enforcement histories accessible to the public.
Looking at the 50 records on this page alone, the severity distribution skews toward 1 critical (Class I-equivalent) actions, 49 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 disclose a unit count, the gap reflects regulatory filing norms where firms disclose lot numbers or distribution channels instead of absolute quantities. This page spans recalls from Mar 8, 2017 to Mar 8, 2017, covering 4 distinct firms. Severity mix is a leading indicator: a page weighted toward critical classifications usually signals an active public-health concern, while lower-severity clusters often represent labeling, undeclared-allergen, or minor design corrections.
Agency-level browsing is useful when a defect pattern crosses categories, for example, a supplier contamination can trigger dozens of downstream recalls that share no obvious product tag but a single issuing agency. Use the pagination below to scan the full archive, or combine this agency filter with category and manufacturer views elsewhere on PlainRecalls to intersect the data. Recall records are sourced directly from FDA Medical Devices's public enforcement feeds and are updated as the agency publishes new notices; the federal record is the authoritative version, and this page aggregates what the agency itself has released. For high-stakes decisions, medical, automotive, or childcare, always click through to the recall detail page and cross-verify the recall number against the agency's current site. Record counts reflect all indexed actions regardless of status (ongoing, terminated, or completed).
Ortho Pack, part number PSS3466(A
Windstone Medical Packaging, Inc.
Orbitofacial Pack, part number AMS5850(A
Windstone Medical Packaging, Inc.
Knee Pack, part number AMS4211
Windstone Medical Packaging, Inc.
Transvaginal Pack, part number CMP1767
Windstone Medical Packaging, Inc.
Major Kit, part number PHC1307(A
Windstone Medical Packaging, Inc.
Total Hip Pack, part number PSS2956
Windstone Medical Packaging, Inc.
Laparotomy Pack, part number 006268-9 Laparotomy Pack, part number AMS4418(A Laparotomy Pack, part number PSS2190(A
Windstone Medical Packaging, Inc.
Laparoscopy Pack (1184), part number AMS6562
Windstone Medical Packaging, Inc.
Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A
Windstone Medical Packaging, Inc.
HSG Pack, part number PSS3287
Windstone Medical Packaging, Inc.
Basic Setup Tray, part number AMS6414
Windstone Medical Packaging, Inc.
Newport Coast Basic Pack, part number 007484-1
Windstone Medical Packaging, Inc.
Arthroscopy Pack, part number AMS6559
Windstone Medical Packaging, Inc.
General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 Gen…
Windstone Medical Packaging, Inc.
TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is i…
Cook Inc.
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, …
Siemens Healthcare Diagnostics, Inc
C-Tray Pack, part number PSS2707(A
Windstone Medical Packaging, Inc.
Basic Pack, part number AMS1868(B Basic Pack, part number AMS2608(A Basic Pack, part number AMS3861 Basic Pack, part number AMS4309 Basic Pack, p…
Windstone Medical Packaging, Inc.
Major Laparotomy Pack - NS, part number AMS4347
Windstone Medical Packaging, Inc.
Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A
Windstone Medical Packaging, Inc.
Custom Venous Kit, part number TVS4024(C
Windstone Medical Packaging, Inc.
D & C Kit, part number CMP1466(A
Windstone Medical Packaging, Inc.
Eye Plastic Tray, part number PSS1931(A
Windstone Medical Packaging, Inc.
Robotic Pack, part number AMS4389
Windstone Medical Packaging, Inc.
Lap Band Pack, part number AMS1785(A
Windstone Medical Packaging, Inc.
Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, …
Siemens Healthcare Diagnostics, Inc
Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pa…
Windstone Medical Packaging, Inc.
Bayview Breast Pack, part number 009080-2
Windstone Medical Packaging, Inc.
Minor Pack, part number AMS3782(B Minor Pack, part number AMS3782(C Minor Pack, part number CMP1560 Minor Pack, part number PSS3518(B Minor Pack,…
Windstone Medical Packaging, Inc.
Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician…
Medtronic Neuromodulation
Major Breast Pack, part number AMS3409(B
Windstone Medical Packaging, Inc.
Lap Chole Pack (6037) , part number AMS6567
Windstone Medical Packaging, Inc.
D&C/Cysto Pack, part number PSS3257(D
Windstone Medical Packaging, Inc.
Hand Tray, part number PSS2365(F Hand Tray, part number PSS2365(G
Windstone Medical Packaging, Inc.
Facial Tray, part number PSS1558(A
Windstone Medical Packaging, Inc.
Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860
Windstone Medical Packaging, Inc.
Foot Pack, part number AMS3637
Windstone Medical Packaging, Inc.
Hip Pack (1347), part number AMS6564
Windstone Medical Packaging, Inc.
Minor Procedure Pack, part number AMS4799
Windstone Medical Packaging, Inc.
Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast …
Windstone Medical Packaging, Inc.
Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.
Cook Inc.
Laminectomy Pack, part number PSS1844(B
Windstone Medical Packaging, Inc.
Morris Hysto Pack, part number PSS3198(A
Windstone Medical Packaging, Inc.
Basic Face Kit, part number PS517A(D
Windstone Medical Packaging, Inc.
Dr. Newman Surgical Procedure Pack, part number PSS1689(A
Windstone Medical Packaging, Inc.
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction o…
Cook Inc.
Anterior Cervical Fusion Pack, part number AMS2502(A Anterior Cervical Fusion Pack, part number AMS2502(C
Windstone Medical Packaging, Inc.
Basic Kit, part number CMP1109(A
Windstone Medical Packaging, Inc.
Minor Tray, part number AMS2685
Windstone Medical Packaging, Inc.
Dr. Casey Pack, part number AMS4313(A
Windstone Medical Packaging, Inc.
Nearby Agencies
Explore recalls from other federal agencies that share oversight of product safety.
Learn More About Recalls
Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Consult a qualified professional before making decisions based on this data.
- Source: FDA Medical Devices - verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index - aggregated from FDA openFDA, CPSC, and NHTSA public databases
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recall counts and figures reflect FDA Medical Devices's own published filings, aggregated alongside the other two federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.