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 161 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 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% 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 5 critical (Class I-equivalent) actions, 45 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 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 Oct 25, 2023 to Nov 1, 2023, covering 18 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).
Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack
Cardinal Health 200, LLC
OPMI LUMERA 300, REF 6137
Carl Zeiss Suzhou Co., Ltd.
PrestiBio Ovulation Strips REF 200-4 60 LH Test Strips
Universal Meditech Inc.
JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6, 10 MM Left, REF 74029262; knee prosthesis
Smith & Nephew, Inc.
Cath Cardiac Pack, REF IHCC03V
American Contract Systems, Inc.
DiagnosUS¿ One Step FSH Menopausal Test (Strip) REF 210-07
Universal Meditech Inc.
PrestiBio Ovulation and Pregnancy Strips REF 100-4 and REF 200-4 60 LH Test Strips/+30 HCF Test Strips
Universal Meditech Inc.
DiagnosUS hCG Pregnancy Urine Test Cassette Format REF 100-13
Universal Meditech Inc.
Robotics Pack, REF SSRO22D
American Contract Systems, Inc.
DiagnosUS One Step LH Ovulation Test Strip REF 200-07
Universal Meditech Inc.
Omega Medical Imaging Elevating Monitor Suspension Systems, Part Number 1000-0085
Omega Medical Imaging, Inc.
DiagnosUS hCG Pregnancy Serum/Urine Test Cassette Format REF 100-27
Universal Meditech Inc.
Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack
Cardinal Health 200, LLC
HealthyWiser UriTest" UTI Test Strips REF 900-UTI
Universal Meditech Inc.
DiagnosUS hCG Pregnancy Urine Test Strip Format REF 100-12
Universal Meditech Inc.
Sub Q Recorder Pack, REF BPRC87A
American Contract Systems, Inc.
JOURNEY II BCS ARTICULAR INSERT, LEFT 10 MM SIZE 5-6, REF 74027262; knee prosthesis
Smith & Nephew, Inc.
HealthyWiser pH-Aware pH 4.5 - 9.0 pH Test Strips REF 900-1P 120 STRIP
Universal Meditech Inc.
Grafton DBM Matrix Strips, Model Numbers: a) T42275, b) T42280; Demineralized Bone Matrix
Medtronic Sofamor Danek USA Inc
DiagnosUS Ovulation Predictor Midstream REF 200-17
Universal Meditech Inc.
Breast Plastics Pack, REF BBPL20D
American Contract Systems, Inc.
Lem Fertility LH Ovulation Test (Strip) REF 200-07
Universal Meditech Inc.
One Step Ovulation Test REF 200-01
Universal Meditech Inc.
Embrace2- Indicated for use as an adjunct to seizure monitoring of adults and children age 6 and up in home or healthcare facilities during periods o…
EMPATICA SRL
Centricity Universal Viewer Workflow Manager, Image processing radiological system
GE Healthcare
HealthyWiser KetoFast" Ketone Test Strips REF 900-1K 150 test strips
Universal Meditech Inc.
Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Preat Corp
Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack
Cardinal Health 200, LLC
Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only. Dental
Preat Corp
To Life hCG Pregnancy Urine Test Strips Format REF Cat No: 100-10
Universal Meditech Inc.
PrestiBio BREAST MILK ALCOHOL TEST STRIP REF 910-10 25 TESTS
Universal Meditech Inc.
Pediatric Urology Wolson Pack, REF BPPU55A
American Contract Systems, Inc.
General Pack, REF BBGP31C
American Contract Systems, Inc.
Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Preat Corp
Am I Pregnant? One Step HCG Pregnancy Test REF 100-17
Universal Meditech Inc.
Centricity PACS-IW, software versions V3.7.x through 3.7.3.9 SP3; Radiological Image Processing System
GE Healthcare
PrestiBio Pregnancy Strips REF 100-4 25 HCG Test Strips
Universal Meditech Inc.
Grafton DBM Crunch, Model Numbers: T44115, Demineralized Bone Matrix
Medtronic Sofamor Danek USA Inc
Olympus High-Flow Insufflation Unit, Model UHI-4. For laparoscopic surgery.
Olympus Corporation of the Americas
SenSight Connector Plug, Model Number B31061.
Medtronic Neuromodulation
stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502
Tornier, Inc
Sapphire Infusion Pumps, Models: Multi-Therapy (REF 15031-000-0028), Epidural (REF 15032-000-0027) and SapphirePlus (REF 15038-000-0001)
EITAN MEDICAL LTD
Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
Cardinal Health 200, LLC
MEDLINE ReNewal Harmonic ACE+7 Shears w/ Adv. Hemostasis Use Only w/ GEN11 SW v2018-1 and Lower, REF HARH45R. surgical instrument.
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument
MEDLINE INDUSTRIES, LP - Northfield
HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002
Access Vascular, Inc
HydroPICC 5Fr Dual Lumen Maximal Barrier Kit, Product Model Number 80002004
Access Vascular, Inc
Functional MR V1.0
OLEA MEDICAL
DeRoyal Head and Neck procedure kit, REF 89-4473, surgical convenience kit
DeRoyal Industries Inc
MEDLINE ReNewal Ligasure Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF4418CR. electrosurgical instrument
MEDLINE INDUSTRIES, LP - Northfield
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
Read our methodology — how this data is sourced, computed, and verified.