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 380 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 1 critical (Class I-equivalent) actions, 46 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 Jul 31, 2019 to Aug 7, 2019, 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).
1 pc Full Wrap Support Belt Apron, Product Number F111, Part Numbers MTREF111*F, MTREF111E, MTREF111F, REF111*F, REF111*M, REF111B, REF111E, REF111F,…
Burlington Medical, LLC
Thyroid Collar, Velcro Closure, Product Number TS2, Part Numbers RBTS2-R, RETS2-R, RLTS2PED, RLTS2-R, RLTS2-SEP, RLTS2-T2T, SBTS2-R, SETS2-R, SLTS2-R…
Burlington Medical, LLC
Frontal Stretch Buckle Closure Apron, Product Number A-10, Part Numbers REA10A, REA10B, REA10C, REA10*F, REA10*M, UEA10*M Product Usage: Products…
Burlington Medical, LLC
Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
Centurion Medical Products Corporation
1 pc Full Wrap Back Relief Apron, Product Number B52 Front & Back Apron, Part Numbers SEB52*F, UEB52*M Product Usage: Products are designed to pr…
Burlington Medical, LLC
BrightView XCT , Model Number 882482
Philips Medical Systems (Cleveland) Inc
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
Terumo Medical Corporation
AXIOM Artis dTC, Model Number 7413078
Siemens Medical Solutions USA, Inc
Terumo Needle, 23G x 1", Product Code NN2325R
Terumo Medical Corporation
Merge OrthoPACS versions 7.3, 7.3.1, 8.0 and 8.0.1
Merge Healthcare, Inc.
Terumo Sur-vet Needle, 20G x 1", Product Code 100204
Terumo Medical Corporation
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
Becton Dickinson & Company
AXIOM Artis FA, Model Number 5904441
Siemens Medical Solutions USA, Inc
Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664
Cardinal Health 200, LLC
Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508
Cardinal Health 200, LLC
Artis zee floor MN, Model Number 10094142
Siemens Medical Solutions USA, Inc
MAC VU360, Model Number 2030360-001, Electrocardiograph
GE Healthcare, LLC
Monoject Standard Hypodermic Needle Item code: 8881200029
Cardinal Health 200, LLC
C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sample bonds to the specific an…
Abbott Laboratories, Inc
ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem when used for the quantit…
Abbott Laboratories
Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
Cardinal Health 200, LLC
MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carto…
Zevex Incorporated (dba MOOG Medical Devices Group)
AXIOM Artis dMP, Model Number 7555365
Siemens Medical Solutions USA, Inc
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 31129344 …
Epimed International, Inc.
AXIOM Artis dBC, Model Number 7728392
Siemens Medical Solutions USA, Inc
POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUT…
Bard Peripheral Vascular Inc
Artis zee ceiling, Model Number 10094137
Siemens Medical Solutions USA, Inc
Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322
Cardinal Health 200, LLC
GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device intended for use in the …
Xcision Medical Systems, LLC
Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011
Cardinal Health 200, LLC
ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are for the estimation of test precision and the detection of systematic analy…
Abbott Laboratories
STANLEY Healthcare Arial 54315 Network Manager
Stanley Security Solutions Inc
AXIOM Artis dBA, Model Number 7555357
Siemens Medical Solutions USA, Inc
AXIOM Artis dFA, Model Number 7555373
Siemens Medical Solutions USA, Inc
Terumo Sur-vet Needle, 22G x 1", Product Code 100211
Terumo Medical Corporation
Artis zee floor, Model Number 10094135
Siemens Medical Solutions USA, Inc
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Medela Inc
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
Terumo Medical Corporation
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Becton Dickinson & Company
Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum or plasma. Antigen in the sam…
Abbott Laboratories, Inc
AXIOM Artis dTA, Model Number 7008605
Siemens Medical Solutions USA, Inc
Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determination of apolipoprotein A1 in human serum or plasma. Antibodies to ap…
Abbott Laboratories, Inc
Artis zee biplane, Model Number 10094141
Siemens Medical Solutions USA, Inc
Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
Cardinal Health 200, LLC
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 311291155 …
Epimed International, Inc.
Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobulin A in human serum or plasma. Antigen in the sam…
Abbott Laboratories, Inc
Artis zeego, Model Number 10280959
Siemens Medical Solutions USA, Inc
Terumo Needle, 18G x 1", Product Code NN1825R
Terumo Medical Corporation
Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
Cardinal Health 200, LLC
Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
Cardinal Health 200, 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.