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 387 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 4 critical (Class I-equivalent) actions, 46 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 46 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 Jun 5, 2019 to Jun 12, 2019, covering 22 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).
Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282
Cook Inc.
Pericardiocentesis Catheter Tray, RPN C-PCYS-850, Order # G03284
Cook Inc.
Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part, Product Usage: The Portex …
Smiths Medical ASD Inc.
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 29cm PG Catalog Number:700106003 UPN: H7877001060030 (2)Soler…
Angiodynamics Inc. (Navilyst Medical Inc.)
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical
NxStage PureFlow B Solution, REF RFP-401, M535RPF4010 NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that…
NxStage Medical, Inc.
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQUIRE…
Microbiologics Inc
Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolid…
I.T.S. GmbH
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large
Zimmer Biomet, Inc.
GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 7…
Maquet Cardiovascular Us Sales, Llc
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero Generator Refurbished PG Catalog Number: 12740000D UPN: H78712740000D0 …
Angiodynamics Inc. (Navilyst Medical Inc.)
Prometra Programmable Pump, Cat. No. 11827 For intrathecal infusion.
Flowonix Medical Inc
TLS2 Thermal Ligating Shears, Catalog Number 132-131D
Microline Surgical, Inc.
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV13F
OriGen Biomedical, Inc.
Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device Rx Only Sterile Product Usage: Is a disposable, single use device inte…
Smiths Medical ASD Inc.
Lineum 4.35mm x 28mm Translation Screw, Model No. 14-524728 The Lineum OCT Spine System is intended to provide immobilization and stabilization of…
Zimmer Biomet, Inc.
MRSASelect II, IVD, REF 63758 (20 plates per package). The MRSASelect is indicated for use in conjunction with other laboratory tests and clinica…
Bio-Rad Laboratories, Inc
Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: 70845357041233 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQ…
Microbiologics Inc
CyberKnife M6, Part Numbers: a) 0660000: CyberKnife Treatment Delivery System b) 053101-010: CyberKnife M6 FI Treatment Delivery System c) 053201…
Accuray Incorporated
Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system processing module. The Alin…
Abbott Gmbh & Co. KG
Sterile Nail Nipper, Barrel Spring (I68400), Sterile
Centurion Medical Products Corporation
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide Small
Zimmer Biomet, Inc.
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Becton Dickinson & Company
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium
Zimmer Biomet, Inc.
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV23F
OriGen Biomedical, Inc.
NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with renal replacement therapy sys…
NxStage Medical, Inc.
IntelliVue MX40 Patient Monitor, Product number 865350, Service # USA: 453564262491 and 453564262511 - Product Usage: Used primarily as a traditional…
Philips North America, LLC
Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat. No. 12828, used with Prometra and Prometra II Programmable Pumps. For int…
Flowonix Medical Inc
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including in-vitro diagnostic (IVD) appl…
Leica Microsystems, Inc.
Prometra Programmer (Grand Prime) Software version 2.00.29, Cat. No. 13828, used with Prometra and Prometra II Programmable Pumps. For intrathecal …
Flowonix Medical Inc
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV32F
OriGen Biomedical, Inc.
Prometra II Programmable Pump, Cat. No. 13827 For intrathecal infusion.
Flowonix Medical Inc
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F
OriGen Biomedical, Inc.
IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564615351, an…
Philips North America, LLC
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large
Zimmer Biomet, Inc.
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO (916-3876): a) REF: INC-11196-70, …
Stryker Neurovascular
IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a trad…
Philips North America, LLC
Prometra II Programmable Pump (Clinical), Cat. No. 01827 For intrathecal infusion.
Flowonix Medical Inc
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420321 Phase 3 Femoral Drill Guide Small
Zimmer Biomet, Inc.
CyberKnife VSI, Part Numbers: a) 032500-010: CyberKnife VSI 9.6.x Robotic Radiosurgery System for Japan b) 033000-010: CyberKnife VSI Robotic Rad…
Accuray Incorporated
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero Applicator 19cm PG Catalog Number: 700106002 UPN: H7877001060020 (2)Sol…
Angiodynamics Inc. (Navilyst Medical Inc.)
Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, R…
Stryker Corporation
Maquet Getinge-BEQ-TOP 5502 ECC Pack Material:701051791R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 21502# Med City Childr Material: 701050060
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 15200 OR PACK HMO & RF Material:701050647R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 22701 Material: 701050790
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 41201 ECC 3/8 PUMP PAC Material: 701064867
Maquet Cardiovascular, LLC
Maquet Getinge- BO-TOP 13901 Rapid Response Universal Pk Material: 701054874R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 3502 LVAD 1/4" Material: 701068168
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 37305 1/4+3/8 TABLE LINE Material: 701067577
Maquet Cardiovascular, LLC
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
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.