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 393 of 782

Official website →

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 3 critical (Class I-equivalent) actions, 47 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 May 29, 2019 to May 29, 2019, 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 May 29, 2019

Drill, contra-angle, 1.5x85mm, Item Number 502015706

Zimmer GmbH

Critical May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid management through the use…

Edwards Lifesciences, LLC

Moderate May 29, 2019

Drill, cannulated, 3x90mm, AO, Item Number 502015631

Zimmer GmbH

Moderate May 29, 2019

CBS micro, countersink, cannulated, AO, Item Number 503004541

Zimmer GmbH

Moderate May 29, 2019

AURIGA XL 4007 BRAZIL SYSTEM Model: M0068FS4007B0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a …

Boston Scientific Corporation

Moderate May 29, 2019

Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635

Zimmer GmbH

Moderate May 29, 2019

AURIGA 30 BRAZIL SYSTEM UPN: M0068S30B0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic…

Boston Scientific Corporation

Moderate May 29, 2019

V-TEK", micro-countersink, round shaft, Item Number 28.66.112

Zimmer GmbH

Moderate May 29, 2019

Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619

Zimmer GmbH

Moderate May 29, 2019

AURIGA 30 GENERAL SYSTEM UPN: M0068S30G0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber opti…

Boston Scientific Corporation

Moderate May 29, 2019

Drill Sys2.7, 2x103mm, AO, Item Number 502015107

Zimmer GmbH

Moderate May 29, 2019

Osteofresh arthrodesis drill, 2x70mm, center tip, AO, 10mm stop, Item Number 502015213

Zimmer GmbH

Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation o…

Remel Inc

Moderate May 29, 2019

AURIGA XL 4007 GENERAL SYSTEM UPN: M0068FS4007G0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fi…

Boston Scientific Corporation

Moderate May 29, 2019

OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tables intended…

Oakworks Inc

Moderate May 29, 2019

Drill, cannulated, 4x90mm, round shaft, Item Number 502015640

Zimmer GmbH

Moderate May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

Zimmer GmbH

Moderate May 29, 2019

Drill, 2.5x94mm, Stryker, Item Number 502015136

Zimmer GmbH

Moderate May 29, 2019

V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111

Zimmer GmbH

Moderate May 29, 2019

Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131

Zimmer GmbH

Moderate May 29, 2019

Drill, 2.5x87mm, AO, Item Number 502015137

Zimmer GmbH

Moderate May 29, 2019

Drill, cannulated, 2x95mm, AO, Item Number ST502015623

Zimmer GmbH

Critical May 29, 2019

MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Drainage System w/Patient Line One Way Valve w Mon…

Integra LifeSciences Corp.

Moderate May 29, 2019

Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable collagen …

Collagen Matrix, Inc.

Moderate May 29, 2019

Drill, 15mm stop, 1x76mm, AO , Item Number 502015115

Zimmer GmbH

Moderate May 29, 2019

Drill, cannulated, 4x150mm, AO, Item Number ST502015403

Zimmer GmbH

Moderate May 29, 2019

CBS micro, countersink, cannulated, AO, Item Number ST503004541

Zimmer GmbH

Critical May 29, 2019

UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under…

Beckman Coulter Inc.

Moderate May 29, 2019

Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630

Zimmer GmbH

Moderate May 29, 2019

NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray sys…

Neusoft Medical Systems Co., Ltd.

Moderate May 29, 2019

AURIGA XL 4007 GENERAL - DEMO SYSTEM UPN: M0068FS4007GD0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System includ…

Boston Scientific Corporation

Moderate May 29, 2019

Drill, 26mm stop, 1.9x94mm, Stryker, Item Number 502015130

Zimmer GmbH

Moderate May 29, 2019

Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number 502015206

Zimmer GmbH

Moderate May 29, 2019

Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207

Zimmer GmbH

Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivat…

Remel Inc

Moderate May 29, 2019

V-TEK", Micro-countersink, AO , Item Number ST28.66.113

Zimmer GmbH

Moderate May 29, 2019

V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111

Zimmer GmbH

Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (18ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation…

Remel Inc

Moderate May 29, 2019

Drill, cannulated, 4x120mm, AO, Item Number 502015402

Zimmer GmbH

Moderate May 29, 2019

NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x…

Neusoft Medical Systems Co., Ltd.

Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivatio…

Remel Inc

Moderate May 29, 2019

V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634

Zimmer GmbH

Moderate May 29, 2019

Drill, cannulated, 2.5x95mm, round shaft, Item Number 502015620

Zimmer GmbH

Moderate May 29, 2019

MaxiCan 4.5 countersink, cannulated, AO, Item Number 503004177

Zimmer GmbH

Moderate May 29, 2019

Drill for 2.7mm screw, 2x125mm, Stryker, Item Number 502015211

Zimmer GmbH

Moderate May 29, 2019

VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro diagnostic use only. The…

Ortho-Clinical Diagnostics

Moderate May 29, 2019

Drill, 2.7x125mm, AO , Item Number ST502015217

Zimmer GmbH

Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (9ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation …

Remel Inc

Moderate May 29, 2019

Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015146

Zimmer GmbH

Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivati…

Remel Inc

Nearby Agencies

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

Compare FDA Medical Devices with FDA Food 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.

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.