PlainRecalls
2023 data Federal recall API Linked to agency record

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 527 of 782

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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 0 critical (Class I-equivalent) actions, 50 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 10 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).

Moderate Mar 8, 2017

Lap Minor Pack (1346), part number AMS6566

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Set-Up Pack, part number PSS1305(C

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Laparoscopic Pack, part number AMS2499 Laparoscopic Pack, part number AMS2499(A Laparoscopic Pack, part number AMS2499(B

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Open Procedure Pack II, part number RMS1740(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Basic Tray, part number PSS1559(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Head/Neck Pack, part number AMS6121

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Shoulder Pack, part number AMS2936 Shoulder Pack, part number AMS3638 Shoulder Pack, part number AMS3711(B Shoulder Pack, part numbere AMS4212 Sh…

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

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

Moderate Mar 8, 2017

Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y Mandible Onlay - Medium - Right

Matrix Surgical Holdings, LLC

Moderate Mar 8, 2017

Extremity Pack, part number AMS3240 Extremity Pack, part number AMS4764 Extremity Pack, part number AMS4788(A Extremity Pack, part number PSS1798(…

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Reduction Mammoplasty Pack, part number AMS4380 Reduction Mammoplasty Pack, part number AMS4380(B

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Augmentation Pack, part number AMS6370

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352. Used to hold the disc segment…

Synthes (USA) Products LLC

Moderate Mar 8, 2017

General Plastics Pack, part number 008617-1

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Liposuction Pack, part number AMS3323(B Liposuction Pack, part number AMS5684 Liposuction Pack, part number AMS5699

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Total Knee Pack (15710), part number AMS6563

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

GYN Pack, part number AMS4013(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163,…

Beckman Coulter Inc.

Moderate Mar 8, 2017

Lap Pack, part number AMS4801

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Ocular Plastic Pack, part number AMS3868(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Opgrande Hand Pack, part number AMS4767

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Hysteroscopy Pack, part number AMS4797 Hysteroscopy Pack, part number AMS4797(A Hysteroscopy Pack, part number AMS4797(B

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Extremity Pack (1344), part number AMS6561

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introducti…

Cook Inc.

Moderate Mar 8, 2017

Chest Breast Drape, part number AMS5853

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and tr…

Olympus Corporation of the Americas

Moderate Mar 8, 2017

Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part number AMS6472

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope

Olympus Corporation of the Americas

Moderate Mar 8, 2017

Shoulder Arthroscopy Pack, part number AMS2496(A Shoulder Arthroscopy Pack, part number AMS2496(B Shoulder Arthroscopy Pack, part number AMS2496(C …

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

EliA Sample Diluent, Article number, 83-1023-01

Phadia US Inc

Moderate Mar 8, 2017

Basic Setup Pack, part number AMS1787(A Basic Setup Pack, part number AMS6519

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Basin Pack, part number AMS2497

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Hystero Pack, part number PSS3535(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Eye Tray, part number PSS1834 Eye Tray, part number PSS1834(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Catheter Pack, part number AMS4399(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external batter…

MED-EL Elektromedizinische Gereate, Gmbh

Moderate Mar 8, 2017

Check-Flo Introducer Hausdorf-Lock Atrial, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for int…

Cook Inc.

Moderate Mar 8, 2017

Lipo Pack, part AMS4420(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Ortho Minor Pack, part number AMS3710(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Lap/Pelviscopy Pack, part number PSS3256(B

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

General Laparoscopy Pack, part number AMS4798 General Laparoscopy Pack, part number AMS4798(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

D & C Pack, part number AMS4796(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access …

Cook Inc.

Moderate Mar 8, 2017

CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 …

Maquet Datascope Corp - Cardiac Assist Division

Moderate Mar 8, 2017

General Plastic Pack, part number PSS2432(A

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Bleph Pack, part number AMS3325(B

Windstone Medical Packaging, Inc.

Moderate Mar 8, 2017

Basic Extended Pack, part number AMS4421(A Basic Extended Pack, part number AMS4421(B

Windstone Medical Packaging, Inc.

Nearby Agencies

Explore recalls from other federal agencies that share oversight of product safety.

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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.

Compiled from official public sources by the editorial team.

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.