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
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).
Drill, contra-angle, 1.5x85mm, Item Number 502015706
Zimmer GmbH
EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid management through the use…
Edwards Lifesciences, LLC
Drill, cannulated, 3x90mm, AO, Item Number 502015631
Zimmer GmbH
CBS micro, countersink, cannulated, AO, Item Number 503004541
Zimmer GmbH
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
Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635
Zimmer GmbH
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
V-TEK", micro-countersink, round shaft, Item Number 28.66.112
Zimmer GmbH
Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619
Zimmer GmbH
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
Drill Sys2.7, 2x103mm, AO, Item Number 502015107
Zimmer GmbH
Osteofresh arthrodesis drill, 2x70mm, center tip, AO, 10mm stop, Item Number 502015213
Zimmer GmbH
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
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
OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tables intended…
Oakworks Inc
Drill, cannulated, 4x90mm, round shaft, Item Number 502015640
Zimmer GmbH
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Zimmer GmbH
Drill, 2.5x94mm, Stryker, Item Number 502015136
Zimmer GmbH
V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111
Zimmer GmbH
Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131
Zimmer GmbH
Drill, 2.5x87mm, AO, Item Number 502015137
Zimmer GmbH
Drill, cannulated, 2x95mm, AO, Item Number ST502015623
Zimmer GmbH
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.
Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable collagen …
Collagen Matrix, Inc.
Drill, 15mm stop, 1x76mm, AO , Item Number 502015115
Zimmer GmbH
Drill, cannulated, 4x150mm, AO, Item Number ST502015403
Zimmer GmbH
CBS micro, countersink, cannulated, AO, Item Number ST503004541
Zimmer GmbH
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.
Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630
Zimmer GmbH
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.
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
Drill, 26mm stop, 1.9x94mm, Stryker, Item Number 502015130
Zimmer GmbH
Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number 502015206
Zimmer GmbH
Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207
Zimmer GmbH
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
V-TEK", Micro-countersink, AO , Item Number ST28.66.113
Zimmer GmbH
V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111
Zimmer GmbH
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
Drill, cannulated, 4x120mm, AO, Item Number 502015402
Zimmer GmbH
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.
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
V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634
Zimmer GmbH
Drill, cannulated, 2.5x95mm, round shaft, Item Number 502015620
Zimmer GmbH
MaxiCan 4.5 countersink, cannulated, AO, Item Number 503004177
Zimmer GmbH
Drill for 2.7mm screw, 2x125mm, Stryker, Item Number 502015211
Zimmer GmbH
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
Drill, 2.7x125mm, AO , Item Number ST502015217
Zimmer GmbH
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
Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015146
Zimmer GmbH
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.
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.