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 442 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, 48 moderate recalls, and 2 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 43 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 Jul 11, 2018 to Jul 18, 2018, covering 15 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).
FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort Defiance Industries Automated …
Fort Defiance Industries, LLC
VPS Rhythm ECG Accessory Pack with Johans Adapter, REF RHY-100-ECGJ Product Usage: To provide real time tip location information of a central ven…
Arrow International Inc
da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System (da Vinci X Surgical System …
Intuitive Surgical, Inc.
GE Healthcare CARESCAPE Monitor B650
GE Healthcare Finland Oy
microTargeting" STar" Drive System (Manual), Product Number ST-DS-MA
FHC, Inc.
microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA
FHC, Inc.
Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Medtronic Inc.
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Beaver Visitec
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 13.5; 00-7713-013-00
Zimmer Biomet, Inc.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Howmedica Osteonics Corp.
microTargeting" Drive System, Product Number MT-DS
FHC, Inc.
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Implant Direct Sybron Manufacturing, LLC
Zimmer¿ M/L Taper Hip Prosthesis With Kinectiv¿ Technology Cementless, Size 6; 00-7713-006-00
Zimmer Biomet, Inc.
LFIT Anatomic CoCr Femoral Heads, 6260-9-036
Howmedica Osteonics Corp.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
Howmedica Osteonics Corp.
Zimmer¿ M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Standard Offset; 00-7711-004-10
Zimmer Biomet, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 16.25; 00-7713-016-00
Zimmer Biomet, Inc.
ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping cas…
ECOLAB INC
microTargeting" Drive System, Product Number 66-ZD-MD
FHC, Inc.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-336
Howmedica Osteonics Corp.
Ratcheting Cannulated Driver Handle, Catalog #: 210-00-004, Rx Only, Non Sterile
Trilliant Surgical Ltd.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 20; 00-7713-020-00
Zimmer Biomet, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinectiv¿ Technology Cementless, Size 5; 00-7713-005-00
Zimmer Biomet, Inc.
microtargeting" Depth Stop Adapter, Product Model Number, Product Number 66-AC-DS(1.8),
FHC, Inc.
ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping ca…
ECOLAB INC
microTargeting" Drive System, Product Number MT-DS-01
FHC, Inc.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144
Howmedica Osteonics Corp.
microTargeting" STar" Drive System (Motorized) Distributed by Medtronic, Product Number FC8002
FHC, Inc.
26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
B. Braun Medical, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 12.5; 00-7713-012-00
Zimmer Biomet, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 15; 00-7713-015-00
Zimmer Biomet, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 7.5; 00-7713-007-00
Zimmer Biomet, Inc.
microTargeting" Lead Adapter for microTargeting" Drive, Product Number 66-CN-DB
FHC, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 17.5; 00-7713-017-00
Zimmer Biomet, Inc.
microTargeting" Drive System Distributed by Medtronic, Product Number 9033G0601
FHC, Inc.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140
Howmedica Osteonics Corp.
Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E Product CVCs are intended to permit venous access to the cen…
Arrow International Inc
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnos…
St Jude Medical Inc.
microTargeting" STar" Drive System (Manual) Distributed by Medtronic, Product Number FC8001
FHC, Inc.
microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB
FHC, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 9; 00-7713-009-00
Zimmer Biomet, Inc.
microTargeting" Drive System, Product Number 66-ZD-MD-01
FHC, Inc.
Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, a…
St Jude Medical Inc.
microTargeting" Drive System Distributed by Medtronic, Product Number FC1006
FHC, Inc.
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 11; 00-7713-011-00
Zimmer Biomet, Inc.
Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
Terumo Medical Corp
microTargeting" STar" Drive System (Motorized), Product Number 70-ZD-ME
FHC, Inc.
Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile
Trilliant Surgical Ltd.
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
Howmedica Osteonics Corp.
Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Extended Offset, 00-7711-004-40
Zimmer Biomet, 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.