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
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).
Compact Speed Reducer, 60:1
The Anspach Effort, Inc.
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
6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system
The Anspach Effort, Inc.
7.5cm QD Angle Attachment
The Anspach Effort, Inc.
10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system
The Anspach Effort, Inc.
Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.
Terumo Medical Corporation
10.5cm Long Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
9.4CM MICRO REVISION ATTACH, BLACK MAX
The Anspach Effort, Inc.
CONTRA ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
ADJUSTABLE DRILL GUIDE, BLACK MAX
The Anspach Effort, Inc.
Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system
The Anspach Effort, Inc.
8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
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
Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V
Sonesta Medical Ab
GREEN ROTATING CRANIOTOME, BLACK MAX
The Anspach Effort, Inc.
7.5CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
SurFlo IV Catheter
Terumo Medical Corporation
14CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
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
System Console, Single Port, no irrigation
The Anspach Effort, Inc.
12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)
Smith & Nephew, Inc.
45 degree Contra Angle Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
90 DEG RIGHT ANGLE ATTACH, BLACK MAX
The Anspach Effort, Inc.
Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system
The Anspach Effort, Inc.
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. …
Boston Scientific Corporation
IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10, REF 71369310, STERILE R, QTY: (1)
Smith & Nephew, Inc.
eMax2 Motor Assembly Product Usage: Electric system
The Anspach Effort, Inc.
16CM MIN INVASIVE ATTACH, BLACK MAX
The Anspach Effort, Inc.
AL-III-DISS Adapter Product Usage: Pneumatic system
The Anspach Effort, Inc.
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
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND…
PEROUSE MEDICAL
11CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
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.
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
eMax2 Hybrid Hand Control Product Usage: Electric system
The Anspach Effort, Inc.
Compact Speed Reducer, 60:1 Black Max
The Anspach Effort, Inc.
Electronic Foot Control with Direction Switch Product Usage: Electric system
The Anspach Effort, Inc.
10.5cm QD Angle Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
IMRI MOTOR Product Usage: Pneumatic system
The Anspach Effort, Inc.
Foot Control, SC2100 Product Usage: Electric system
The Anspach Effort, Inc.
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.
22CM MICRO REVISION ATTACH, BLACK MAX
The Anspach Effort, Inc.
Autolube-III with NK Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)
Smith & Nephew, Inc.
Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
The Anspach Effort, Inc.
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.
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.
AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
The Anspach Effort, 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.
- 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.