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 392 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 4 critical (Class I-equivalent) actions, 46 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 12 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, cannulated, 3x90mm, AO, Item Number ST502015631
Zimmer GmbH
Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7 Fr 003500 G14916; 6.0 Fr 003600 G14836; 7.0 Fr 003700 G1483…
Cook Inc.
CBS micro, countersink, cannulated, round-shaft, Item Number 503004341
Zimmer GmbH
Drill, 15mm stop, 1x83mm, Stryker, Item Number 502015114
Zimmer GmbH
AURIGA 30 BRAZIL ZERO COST SYSTEM UPN: M0068S30BZ0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a …
Boston Scientific Corporation
Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultiva…
Remel Inc
Drill, cannulated, 2.5x95mm, AO, Item Number 502015621
Zimmer GmbH
UniCel DxH 800 Coulter Cellular Analysis System, REF numbers 629029, B24465, B24802, B68304, B66445, and B63322. Product Usage: The UniCel DxH 80…
Beckman Coulter Inc.
Drill for 3.5mm screw, 2.5x120mm, AO, Item Number ST502015216
Zimmer GmbH
Drill, cannulated, 2.8x150mm, AO, Item Number 502015629
Zimmer GmbH
V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, AO, Item Number 502015638
Zimmer GmbH
CHOL+HDL+GLU test strips, REF 2412
Polymer Technology Systems, Inc.
Drill, cannulated, 3x90mm, round shaft, Item Number 502015630
Zimmer GmbH
CBS 4.0 countersink, cannulated, 15mm stop, AO, Item Number 503004352
Zimmer GmbH
Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600 micron single use fiber K2011824 600 mi…
Dornier Medtech America, Inc.
EDS Light Suspension, Central Axis, a component of the Stryker Visum LED Surgical Lighting System, with the following catalog numbers: 0682001286, E…
Stryker Communications
Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN: 4.0 Fr - SIPSF-040018-56-6 G18168 4.0 Fr - SIPSF-040018-59 …
Cook Inc.
Drill, cannulated, 2.8x120mm, AO, Item Number ST502015628
Zimmer GmbH
Drill, cannulated, 4x120mm, AO, Item Number ST502015402
Zimmer GmbH
AURIGA 30 GENERAL ZERO COST SYSTEM UPN: M0068S30GZ0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including …
Boston Scientific Corporation
Drill for 2.7mm screw, 2x120mm, AO, Item Number 502015212
Zimmer GmbH
Drill, 26mm stop, 1.4x94mm, Stryker, Item Number 502015120
Zimmer GmbH
CBS 7.5 tap, cannulated, AO, Item Number 503002041
Zimmer GmbH
Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number ST502015207
Zimmer GmbH
Thio Med w/o Ind, w/Dex (18ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation …
Remel Inc
Adapter for handpiece, guided, reusable, for guide sleeve 0 4.8 mm Article number: 3.04.090 - Product Usage: The adapter for handpiece, guided reus…
Thommen Medical AG
Thio Med w/o Ind, w/Dex (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation …
Remel Inc
Thio Med w/o Ind, w/Dex (10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation…
Remel Inc
Drill for 3.5mm screw, 2.5x120mm, AO, Item Number 502015216
Zimmer GmbH
DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is intended to acquire dental int…
KaVo Dental Technologies LLC
Drill, 26mm stop, 1.4x94mm, stryker, Item Number 502015145
Zimmer GmbH
V-TEK", Micro-countersink, AO, Item Number 28.66.113
Zimmer GmbH
Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife treatment planning.
Elekta Instrument AB
Drill, cannulated, 2x95mm, round shaft, Item Number 502015619
Zimmer GmbH
UniCel DxH 600 Coulter Cellular Analysis System, REF number B23858. Product Usage: Note: The DxH 600 hematology analyzer is the same instrument a…
Beckman Coulter Inc.
CBS high, countersink, cannulated, round-shaft, Item Number 503004342
Zimmer GmbH
Drill, cannulated, 2.8x120mm, AO, Item Number 502015628
Zimmer GmbH
Drill, 2.5x135mm, AO, Item Number 502015142
Zimmer GmbH
Thio Med w/Dex, Hemin, Vit K (5ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivat…
Remel Inc
Lipid Panel test strips (as a component of smart bundles), REF 2729, also private labeled under Henry Schein as REF 570-0412
Polymer Technology Systems, Inc.
Drill, cannulated, 4x90mm, round shaft, Item Number ST502015640
Zimmer GmbH
CBS 4.5 countersink, cannulated, 18mm stop, round-shaft, Item Number 503004351
Zimmer GmbH
MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount System Product Usage: The MoniTorr ICP External CSF Drainage and Monitoring Sy…
Integra LifeSciences Corp.
Drill, 3.2x145mm, AO, Item Number ST502015650
Zimmer GmbH
LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr INS9020SP1 INS-9020SP1 LIMITORR VOLUME EVD 20ML LimiTorr INS9030 INS-9030 LIM…
Integra LifeSciences Corp.
Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultiv…
Remel Inc
Drill, cannulated, 2x95mm, AO, Item Number 502015623
Zimmer GmbH
Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivati…
Remel Inc
Drill, cannulated, 3.5x90mm, round shaft, Item Number ST502015635
Zimmer GmbH
Drill, cannulated, 2.5x95mm, AO, Item Number ST502015621
Zimmer GmbH
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.