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 467 of 782

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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 1 critical (Class I-equivalent) actions, 49 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 46 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 Mar 21, 2018 to Mar 28, 2018, covering 20 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 Mar 28, 2018

WOUND CARE KIT

Centurion Medical Products Corporation

Moderate Mar 28, 2018

GENICON EZEE Retrieval, sterile, Rx only.

Genicon, Inc.

Moderate Mar 28, 2018

INCISION & DRAINAGE TRAY or KIT

Centurion Medical Products Corporation

Moderate Mar 28, 2018

AutoMate 1200 Catalog Number ODL25120; AutoMate 1250 Catalog Number ODL25125; AutoMate 2500 Catalog Number ODL25250; AutoMate 2550 Catalog Number …

Beckman Coulter Inc.

Moderate Mar 28, 2018

TUBING CHANGE KIT

Centurion Medical Products Corporation

Moderate Mar 28, 2018

J-Plasma Precise(R) OPEN, Catalog Numbers: BVX-044-BPP, BVX-044-BPS, BVX-150-BPP, BVX-150-BPS

Bovie Medical Corporation

Moderate Mar 28, 2018

WOUND CLOSURE TRAY - FACIAL

Centurion Medical Products Corporation

Moderate Mar 28, 2018

12F MODIFIED Tesio CATHETER SET, REF MCTC1235SM, UDI 884908027259 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged…

Medical Components, Inc dba MedComp

Moderate Mar 28, 2018

Custom Dialysis Kit CF-4235 Without Gel, which includes Flex-Neck¿ Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # K14-00079

Merit Medical Systems, Inc.

Critical Mar 28, 2018

BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI: 50382903664509); 3. 366643 (UDI: 5038290366…

Becton Dickinson & Company

Moderate Mar 28, 2018

SKIN STAPLE REMOVER

Centurion Medical Products Corporation

Moderate Mar 28, 2018

Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # CF-4235/B

Merit Medical Systems, Inc.

Moderate Mar 28, 2018

Re-Entry" Malecot Nephrostomy Catheter Set, Product Number: M0064101040, GTIN: 08714729008446 The Malecot Nephrostomy Catheter Set is intended to…

Boston Scientific Corporation

Moderate Mar 28, 2018

ARROWg+ard Blue PLUS catheter, Catalog Number: ASK-45854-NG Product Usage: The ARROWg+ard Blue PLUS¿ catheter permits venous access to central ci…

Arrow International Inc

Moderate Mar 28, 2018

Malecot Nephrostomy Catheter Set, Product Number: M0064101010, GTIN: 08714729005278 The Malecot Nephrostomy Catheter Set is intended to establish…

Boston Scientific Corporation

Moderate Mar 28, 2018

Custom Dialysis Kit CF-4230 Without Gel, which includes Flex-Neck¿ Classic Peritoneal Dialysis Catheter 2 Cuffs Infant Coiled, Catalog # K14-00078

Merit Medical Systems, Inc.

Moderate Mar 28, 2018

smith&nephew, LEGION HK FEMORAL WEDGE (WEDGE AND SCREW), 5 MM, SIZE 5, REF 71422159, QTY: (1), STERILE The Revision Knee System Components are in…

Smith & Nephew, Inc.

Moderate Mar 28, 2018

PEDIATRIC IV & IV START KIT

Centurion Medical Products Corporation

Moderate Mar 28, 2018

Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical 2 MHz Waterproof OB probe is for obstetrical use in the labor and department…

CooperSurgical, Inc.

Moderate Mar 28, 2018

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, a…

Arrow International Inc

Moderate Mar 28, 2018

Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Per…

Arrow International Inc

Moderate Mar 28, 2018

ST. CHRISTOPHER'S SECUREMENT SET

Centurion Medical Products Corporation

Moderate Mar 28, 2018

Iridex TruFocus LIO Premiere" Laser Indirect Ophthalmoscope ( LIO ) The LIO is a headmounted indirect ophthalmoscope which is used with a handh…

Iridex Corporation

Moderate Mar 28, 2018

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maxi…

Arrow International Inc

Moderate Mar 28, 2018

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. P…

Arrow International Inc

Moderate Mar 28, 2018

CIRCUMCISION TRAY

Centurion Medical Products Corporation

Moderate Mar 28, 2018

Pressure Injectable Multi- Lumen CVC Kit

Arrow International Inc

Moderate Mar 21, 2018

PORT-A-CATH II PS/Titan, Tray PAC II. Labeled as: a. VEN LP, PU, 2.6MM, UL, 8.5FR/INTRO (1/EA); b. DL, LP, PU, 2.2MM, WING-LOCK, 7FR/INTRO …

Smiths Medical ASD Inc.

Moderate Mar 21, 2018

NovaKone Toric Daily Wear Soft contact; Catalog Number: AONKT54 Product Usage: The NOVAKONE TORIC lens is indicated for daily wear for persons re…

Alden Optical

Moderate Mar 21, 2018

CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented

Zimmer Biomet, Inc.

Moderate Mar 21, 2018

VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Zimmer Biomet, Inc.

Moderate Mar 21, 2018

LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and dis…

Zimmer Biomet, Inc.

Moderate Mar 21, 2018

Coons Interventional Wire Guide

Cook Inc.

Moderate Mar 21, 2018

Movable Core Wire Guide

Cook Inc.

Moderate Mar 21, 2018

STA - Neoplastine¿ Cl Plus ¿ (ref. 00606) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

Moderate Mar 21, 2018

BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematology determina…

Becton Dickinson & Company

Moderate Mar 21, 2018

MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number: 8888222316.

Medtronic Minimally Invasive Therapies Group

Moderate Mar 21, 2018

ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) centr…

Arrow International Inc

Moderate Mar 21, 2018

Neoplastine¿ Cl Plus ¿ (ref. 00375) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

Moderate Mar 21, 2018

CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR OPTION FEM COMP SIZE D/L CR OPTION FEM COMP SIZE D/R CR OPTION FEM COMP SIZE E/L CR O…

Zimmer Biomet, Inc.

Moderate Mar 21, 2018

Amplatz Extra Stiff Wire Guide

Cook Inc.

Moderate Mar 21, 2018

STA - Neoplastine¿ Cl ¿ (ref. 00605) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

Moderate Mar 21, 2018

ACE (TM) BRAND, DELUXE ANKLE BRACE, 207736, UPC 0 51131 20387 7

3M Company - Health Care Business

Moderate Mar 21, 2018

Amplatz Ultra Stiff Wire Guide

Cook Inc.

Moderate Mar 21, 2018

LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-R LPS-FLEX OPTION FEMORAL D-L LPS-FLEX OPTION FEMORAL D-R LPS-…

Zimmer Biomet, Inc.

Moderate Mar 21, 2018

Bentson Cerebral Wire Guide

Cook Inc.

Moderate Mar 21, 2018

ARROWg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central ve…

Arrow International Inc

Moderate Mar 21, 2018

Vygon IV Start Convenience Kits; Product Codes AMS-623T and AMS-626TGSLF. Kit used when administering IV during emergency.

Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

Moderate Mar 21, 2018

Femoral Artery Pressure Monitoring Set

Cook Inc.

Moderate Mar 21, 2018

Reuter Tip Deflecting Wire Guide

Cook 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.