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 201 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 0 critical (Class I-equivalent) actions, 47 moderate recalls, and 3 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 Dec 28, 2022 to Jan 11, 2023, covering 21 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).
ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445
Biomerieux Inc
VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS, CATALOG 413404
Biomerieux Inc
DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML), CATALOG 306-R1026-01
Biomerieux Inc
API 20 E 25 STRIPS, CATALOG 20100
Biomerieux Inc
9 Gauge Disposable Trocars with Blunt Pushers for Use with Subcutaneous Implants Part Number: 50134-01
ENDO Pharmaceuticals Solutions, Inc.
VIDAS CLINICAL VIDAS PROGESTERONE 60 TESTS, CATALOG 30409-01
Biomerieux Inc
VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended for use in installation testing and routine moni…
Steris Corporation
API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500
Biomerieux Inc
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
Remington Medical, Inc.
Pilling Wecksorb Cylindrical Sponges
TELEFLEX LLC
Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - 5.5 Screw 30-0021-S 25.0mm Acutrak 2¿ - 5.5 Screw 30-0023 30.0mm Acutrak 2¿ -…
Acumed LLC
Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm Dual-Trak Clavicle Screw 40-0136-S 3.0mm x 80mm Dual-Trak Clavicle Sc…
Acumed LLC
AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S 10mm AcuTwist¿ Acutrak Compression Screw AI-0012-S 12mm AcuTwist¿ Acut…
Acumed LLC
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw AM-0030-S 30.0mm …
Acumed LLC
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Young Dental Manufacturing I, LLC
Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Baxter Healthcare Corporation
VADER Pedicle System Torque Wrench, Hudson Coupling, 12 Nm, REF 42-702
Icotec Ag
Revaclear 400 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Baxter Healthcare Corporation
Full Dose CE Simplex P Single Bone Cement - Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number: 6191-0-001
Howmedica Osteonics Corp.
HeartWare Model 1100
Heartware, Inc.
Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid…
GE Medical Systems, LLC
ConvaTec AQUACEL Foam Ag Adhesive, wound dressing advesive
ConvaTec, Inc
Vivid S5 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ…
GE Medical Systems, LLC
Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
Corin Ltd
HeartWare HVAD Pump Kit, REF 1104CA-CLIN
Heartware, Inc.
HeartWare Model 1101
Heartware, Inc.
DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q
DeVilbiss Healthcare LLC
Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid…
GE Medical Systems, LLC
Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139, K061525, K082374, K092140, K102388, K121062). Used in ultrasound imagin…
GE Medical Systems, LLC
Tobra Full Dose CE Antibiotic Simplex P- Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number:6197-1-001
Howmedica Osteonics Corp.
Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
Tomy International Inc.
Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215
Corin Ltd
2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute and chronic dialysis therapy in a healthcare facility Models: (1) 19071…
Fresenius Medical Care Holdings, Inc.
HeartWare HVAD Pump Kit, REF 1103
Heartware, Inc.
Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-096
Abbott Molecular, Inc.
B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,
GE Medical Systems, LLC
B125M Patient Monitor, REF 6160000-004-XXXXXX
GE Medical Systems, LLC
Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging sources.
GE Medical Systems, LLC
HeartWare HVAD Pump Kit, REF 1104
Heartware, Inc.
Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
Medical Action Industries, Inc. 306
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Medical Action Industries, Inc. 306
Vivid q ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid)…
GE Medical Systems, LLC
The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm ran…
PHONESOAP
Vivid q N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Orga…
GE Medical Systems, LLC
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
NuVasive Inc
B125P Patient Monitor (with E-module slot option), REF 6160000-002
GE Medical Systems, LLC
HeartWare HVAD Pump Kit, REF MCS1705PU
Heartware, Inc.
B105M Patient Monitor, REF 6160000-003
GE Medical Systems, LLC
Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090
Abbott Molecular, Inc.
Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the USA. Used to treat chronic and acute renal failure by hemodialysis.
Baxter Healthcare Corporation
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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.