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 71 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 83,949 records spanning 1995 through 2026, FDA Medical Devices accounts for roughly 46.6% 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 6 critical (Class I-equivalent) actions, 44 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 48 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 19, 2025 to Mar 26, 2025, 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).
Proxima Drape labeled as MINOR PACK and LAPAROSCOPY. Sterile surgical drape.
MEDLINE INDUSTRIES, LP - Northfield
THORACIC PACK , Model No UTTC82Y UTTC82AA-01
American Contract Systems Inc
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, with Component PCB, TSI/RSI firmware C29278
Beckman Coulter, Inc.
BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF: 1116-00, CII Safe ES Deskt…
CareFusion 303, Inc.
Access 2 Immunoassay Analyzer, Catalog Number 81600N
Beckman Coulter, Inc.
Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape.
MEDLINE INDUSTRIES, LP - Northfield
OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02
American Contract Systems Inc
Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
FUJIFILM Healthcare Americas Corporation
Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC
MEDLINE INDUSTRIES, LP - Northfield
CV BASIC PUMP PACK , Model No WECV23D
American Contract Systems Inc
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
MEDLINE INDUSTRIES, LP - Northfield
IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit; UPN/Catalog Number: ISO-60;
Angiodynamics, Inc.
Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW; SHEET, DRAPE, SPLIT, ST,10/CS; DRAPE,LAPROSCOPY,CHOLE,W/TROUGH,ST,8/CS; DRAPE,LAPROSCOPY,CHOLE,W/…
MEDLINE INDUSTRIES, LP - Northfield
Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 12 mm, Product Code: 880-601/12
Waldemar Link GmbH & Co. KG (Mfg Site)
Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
B Braun Medical Inc
MAJOR DIEP, Model Nos. CCMJ73G-01 CCMJ73H
American Contract Systems Inc
SPINE LUMBAR PACK , Model No UTSL72AA UTSL72AB
American Contract Systems Inc
NEURO IR TRAY , Model No WENI56J
American Contract Systems Inc
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137.
Beckman Coulter, Inc.
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
American Contract Systems Inc
EAR PACK , Model No SFEA12A
American Contract Systems Inc
LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02
American Contract Systems Inc
LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41G
American Contract Systems Inc
smiths medical ProPort Plastic Venous Access System, PolyFlow Catheter, 2.6 (7.8Fr) O.D. x 1.6mm I.D., 8.5Fr Introducer, REF 21-4171-24
Smiths Medical ASD, Inc.
Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H Set Infant/Neonatal, 006147 …
Oridion Medical 1987 Ltd.
TOTAL HIP PACK , Model No SMTH06O SMTH06P
American Contract Systems Inc
smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 2.6mm O.D. (7.8Fr) x 1.6mm I.D., REF 21-4155-24
Smiths Medical ASD, Inc.
smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm (5.8Fr) O.D. x 1.0mm I.D., 6Fr Introducer, REF 21-4153-24
Smiths Medical ASD, Inc.
Proxima Drape labeled as FACE LIFT. Sterile surgical drape.
MEDLINE INDUSTRIES, LP - Northfield
VERICIS, Merge Cardio, Model/Catalog Number: Version 11.x, Software Version: 11.0.2, 11.0.3, 11.0.4, 11.1, 11.1.1; The VERICIS is an integrated cardi…
Merge Healthcare, Inc.
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Stryker Corporation
Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. …
Medtronic Perfusion Systems
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Description: The Powerheart G5 autom…
ZOLL Medical Corporation
CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an Electrophy…
CardioFocus, Inc.
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-…
Aesculap Inc
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C, (6) G5A-13C…
ZOLL Medical Corporation
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
CareFusion 303, Inc.
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
Beckman Coulter, Inc.
Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;
Philips Medical Systems Nederland B.V.
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA P…
ZOLL Medical Corporation
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of in…
Cordis US Corp
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S…
ZOLL Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4) G5A-03A, (5) G5A-19A, (6) G5A-80A…
ZOLL Medical Corporation
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version: NA Product Description: Th…
ZOLL Medical Corporation
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN38-SB Software Version: N/A
TruAbutment Inc.
Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ501R, Phaneuf Hysterectomy Fo…
Aesculap Inc
GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
GE Medical Systems, LLC
Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/…
Smiths Medical ASD, Inc.
Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann Mosquito FCSDEL STR 100MM; …
Aesculap Inc
GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed
GE Medical Systems, LLC
Nearby Agencies
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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
Read our methodology — how this data is sourced, computed, and verified.