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 210 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 2 critical (Class I-equivalent) actions, 47 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 Nov 30, 2022 to Dec 7, 2022, covering 17 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).
Accelerate PhenoTest BC kit REF 10102018
Accelerate Diagnostics Inc
CytoCell BCL11B Proximal in FITC Spectrum-LDT for investigation T-cell related malignancy. This device is an analyte specific reagent probe covering…
Cytocell Ltd.
Alcon Custom Pak Surgical Procedure Pack
Alcon Research, LLC
Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1
Busse Hospital Disposables, Inc.
Trinity Biotech HbA1c (GHb) Contorls Kit, 500uL (Levels I & II), REF 01-04-0020, Part number 05-01-0040B, A1c analysis
Primus Corporation dba Trinity Biotech
GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit fo…
Greer Laboratories, Inc.
Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734
Owens & Minor Distribution, Inc.
CMV IgM EIA, in vitro diagnostic.
Bio-Rad Laboratories, Inc.
regard DAVINCI PACK, GS00137W, Item Number 880132023; gastric surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Small Drape with Adhesive Aperture, REF 1020, general surgery drape
3M Healthcare Business
regard BASIC NEURO, NU00259R, Item Number 800021018; neuro surgery convenience kit
ROi CPS LLC
MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
Beckman Coulter, Inc.
regard RETINAL PACK, EY00935C, Item Number 800730003; EYE surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Large Towel Drape, REF 1010, general surgery drape
3M Healthcare Business
regard NEURO PACK, NU00278L, Item Number 800040012; nuero surgery convenience kit
ROi CPS LLC
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Allison Medical, Inc.
regard BASIC NEURO, NU00259S, Item Number 800021019; neuro surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Medium Drape with Incise Film, REF 1060, general surgery drape
3M Healthcare Business
regard SPINE PACK, NU00260H, Item Number 800022008; ortho surgery convenience kit
ROi CPS LLC
Medfusion Model 4000 Syringe Infusion Pump, with software versions V1.6.0 or V1.6.1 that have implemented the Smart Pump Programming (SPP) feature in…
Smiths Medical ASD Inc.
regard HIP ARTHROSCOPY, OR01092B, Item Number 880462002; ortho surgery convenience kit
ROi CPS LLC
¿regard CV¿PART¿¿1¿BUNDLE¿- MERCY¿ST¿ANTHONY , CV01005H, Item Number 830099008; cardiac surgery convenience kit
ROi CPS LLC
regard CERVICAL PACK, NU00303H, Item Number 800058008; neuro surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Small Towel Drape, REF 1000NSD, general surgery drape
3M Healthcare Business
3M Steri-Drape, Urological Drape, REF 1071, general surgery (urology) drape
3M Healthcare Business
Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002
Whele LLC DBA Perch
K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Kamiya Biomedical Company, LLC
regard SHOULDER PACK, GS00125V, Item Number 880120022; ortho surgery convenience kit
ROi CPS LLC
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
Medical Action Industries, Inc. 306
Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use
Abbott Molecular, Inc.
regard SHOULDER W BCH CHAIR, OR00356F, Item Number 800203006; ortho surgery convenience kit
ROi CPS LLC
regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
ROi CPS LLC
regard FOOT PACK - MERCY SPRINGFIELD , OR00123Z, Item Number 880118026; ortho surgery convenience kit
ROi CPS LLC
regard MINOR NEURO, NU00140AD, Item Number 880135030; neuro surgery convenience kit
ROi CPS LLC
regard ACDF, NU00698H, Item Number 800246008; neuro surgery convenience kit
ROi CPS LLC
Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
Whele LLC DBA Perch
3M Steri-Drape, Large Towel Drape, REF 1010NSD, general surgery drape
3M Healthcare Business
regard SHOULDER, GS00828G, Item Number 880367007; ortho surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Medium Drape with Wide Adhesive Aperture, REF 1033, general surgery drape
3M Healthcare Business
3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030NS, general surgery drape
3M Healthcare Business
regard FOOT PACK, OR00123Y, Item Number 880118; orthopedic surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Large Towel Drape, REF 1010NS, general surgery drape
3M Healthcare Business
3M Steri-Drape, Medium Drape with Incise Film, REF 1060NS, general surgery drape
3M Healthcare Business
regard SHOULDER ARTHROSCOPY, OR01103A, Item Number 880471001; ortho surgery convenience kit
ROi CPS LLC
regard SPINE, OR01100A, Item Number 880468001; ortho surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Small Drape with Incise Film, REF 1021NS, general surgery drape
3M Healthcare Business
regard LATERAL SHOULDER, OR01044C, Item Number 880435003; ortho surgery convenience kit
ROi CPS LLC
regard TOTAL JOINT, OR00446F, Item Number 880291; orthopedic surgery convenience kit
ROi CPS LLC
3M Steri-Drape, Small Towel Drape, REF 1000NS, general surgery drape
3M Healthcare Business
regard HAND PACK, OR00594K, Item Number 800243011; ortho surgery convenience kit
ROi CPS LLC
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
Read our methodology — how this data is sourced, computed, and verified.