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 388 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, 49 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 Jun 5, 2019 to Jun 5, 2019, covering 7 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).
Maquet Getinge- (1)Material: 701065765R01 BO-TOP 36504 Adult ECC Pack (2)Material: 701065765R02 BO-TOP 36504 Adult ECC Pack
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 24202 ADULT ECC Material:701054295
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-TOP 32200 ECC Pack Material: 701053319R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 5208 ECC SET CARDIAC Material: 701067350
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 35503 SGD Pack Material:701068797R01
Maquet Cardiovascular, LLC
Maquet Getinge BO-TOP 48400 OR PACK Material: 701064327R01
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-TOP 28901 MCV INFANT ECC Material:701056771R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 48003 Rotaflow ONLY Support Pack Material:709000490
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 25501 3/8" Better Bladder Pack Material: 709000370
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 44701 PEDIATRIC ECC Material: 701064825
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 5909 1/4 PACK W QPID Material: 701064992
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 8506 Transport Pack Material: 709000146
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 33501 1/4" ECC PACK Material: 701053754
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 38900 ECC PACK Material: 701056368
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 8013 ECC QUADROX iD Pack RF32 Material: 701047962
Maquet Cardiovascular, LLC
Alinity i Processing Module, 03R65 01, with the below components. a. TED (Thermo Electric Device) Engine, Reagent cooler; b. CABLE, POWER OU…
Abbott Gmbh & Co. KG
Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material: 701055388R01
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 28903 Adult ECC Pack Material: 709000093
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 33704 ECC 1/4" PACK Material: 701054150
Maquet Cardiovascular, LLC
Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 51501 Ochsner ECC Pack Material:709000113
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 3502 LVAD 1/4" Material: 701068168R01
Maquet Cardiovascular, LLC
McKesson Cardiology Hemo
Change Healthcare Israel Ltd.
Maquet Getinge- (1) Material: 701067350R01 BEQ-TOP 5208 ECC Small-Cardiac (2) material: 701067350R02 BEQ-TOP 5208 ECC Small-Cardiac
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 9004 1/4 Custom Pk w/RF32 & HMOD Material: 701054451R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 33700 ECC 3/8" PACK Material: 701053845
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 5914 TCH ¿ Inch Change Kit Material: 709000334
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 21502 ECC Quadrox iD w/RF 3/8" Material:701050060R01
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-T 9411 Lurie Children's 1/4 ADAPT Material:709000485R01
Maquet Cardiovascular, LLC
ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, UPC 305733010037 - Product Usage: ThermaCare(R) HeatWraps are indicated in adults to provide heat t…
PF Consumer Healthcare 1 LLC
Maquet Getinge-BEQ-TOP 26402 ECC PACK Material: 701062310
Maquet Cardiovascular, LLC
Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 3700 Tubing Pack Material: 701049510
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 38002 ADULT SPECIALTY Material:
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 37302 Quadrox iD Pediatric Pack Material: 701065190
Maquet Cardiovascular, LLC
Maquet Getinge-BO-T 6600 TUBING PACK Material:701052324
Maquet Cardiovascular, LLC
SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, STFI-1635, STFI-1825, STFI-1835, STFI-192…
Terumo Medical Corporation
Opteform Allograft Disc, 30mm 3mm, 2cc, Catalog Number 600-03-30
Exactech, Inc.
Maquet Getinge-BEQ-T 4917 Mercy Medical Versa-Pack Material: 709000368
Maquet Cardiovascular, LLC
RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
Teleflex Medical
Maquet Getinge-BEQ-TOP 1601#QUADROX iD - Pack Material:701052285
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 37500 ECC QUADROX ID Material: 701055601
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 25001 MONTEFIORE Material: 701053906
Maquet Cardiovascular, LLC
Maquet Getinge- BO-T 41301 BUMC ECC PACK Material: -701065209R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 250011/4 1/4 Less than 20 kg up Material: 701053906R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 51502 Ochsner ECC Ancillary Pack Material:709000115
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 8075 S-Quadrox iD Plus Pack wRF3 Material: 709000460
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 49002 ROTAFLOW SUPPORT PACK Material: 701067280
Maquet Cardiovascular, 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
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.