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 514 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 0 critical (Class I-equivalent) actions, 49 moderate recalls, and 1 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 49 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 10, 2017 to May 10, 2017, covering 11 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 10, 2017

Compact Speed Reducer, 60:1

The Anspach Effort, Inc.

Moderate May 10, 2017

Dressing, Knee L/XL, P/N 04708 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

Moderate May 10, 2017

6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

7.5cm QD Angle Attachment

The Anspach Effort, Inc.

Moderate May 10, 2017

10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.

Terumo Medical Corporation

Moderate May 10, 2017

10.5cm Long Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

9.4CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

CONTRA ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

ADJUSTABLE DRILL GUIDE, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pa…

Breg Inc

Moderate May 10, 2017

Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V

Sonesta Medical Ab

Moderate May 10, 2017

GREEN ROTATING CRANIOTOME, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

7.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

SurFlo IV Catheter

Terumo Medical Corporation

Moderate May 10, 2017

14CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

Dressing Knee/Shldr, P/N 02328 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

Moderate May 10, 2017

System Console, Single Port, no irrigation

The Anspach Effort, Inc.

Moderate May 10, 2017

12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)

Smith & Nephew, Inc.

Moderate May 10, 2017

45 degree Contra Angle Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

90 DEG RIGHT ANGLE ATTACH, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. …

Boston Scientific Corporation

Moderate May 10, 2017

IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10, REF 71369310, STERILE R, QTY: (1)

Smith & Nephew, Inc.

Moderate May 10, 2017

eMax2 Motor Assembly Product Usage: Electric system

The Anspach Effort, Inc.

Moderate May 10, 2017

16CM MIN INVASIVE ATTACH, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

AL-III-DISS Adapter Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy p…

Breg Inc

Moderate May 10, 2017

DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND…

PEROUSE MEDICAL

Moderate May 10, 2017

11CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the …

Merge Healthcare, Inc.

Moderate May 10, 2017

Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy …

Breg Inc

Moderate May 10, 2017

eMax2 Hybrid Hand Control Product Usage: Electric system

The Anspach Effort, Inc.

Moderate May 10, 2017

Compact Speed Reducer, 60:1 Black Max

The Anspach Effort, Inc.

Moderate May 10, 2017

Electronic Foot Control with Direction Switch Product Usage: Electric system

The Anspach Effort, Inc.

Moderate May 10, 2017

10.5cm QD Angle Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

IMRI MOTOR Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

Foot Control, SC2100 Product Usage: Electric system

The Anspach Effort, Inc.

Moderate May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a digital product available …

Roche Diabetes Care, Inc.

Moderate May 10, 2017

22CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

Moderate May 10, 2017

Autolube-III with NK Product Usage: Pneumatic system

The Anspach Effort, Inc.

Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)

Smith & Nephew, Inc.

Moderate May 10, 2017

Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

The Anspach Effort, Inc.

Moderate May 10, 2017

AQUIOS CL Flow Cytometer, Ref no. B30166, Software Versions 2.0 and 2.0.1 Product Usage: The AQUIOS CL Flow Cytometer is intended for use with in…

Beckman Coulter Inc.

Low May 10, 2017

The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is…

Zimmer Trabecular Metal Technology, Inc.

Moderate May 10, 2017

AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system

The Anspach Effort, Inc.

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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.