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 391 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 May 29, 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-BEQ-TOP 50900 Custom ECC Pack-Neonatal ¿ Material: 709000069R02
Maquet Cardiovascular, LLC
Maquet Getinge BO-TOP 28903 Adult ECC Pack Material: -709000093R01
Maquet Cardiovascular, LLC
Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alvarado II Base Plate and Foot Piece: Alvarado Foot Piece: Item Number: 0…
Zimmer Surgical Inc
Maquet Getinge-BEQ-TOP 24105 ECC PACK Material:701064757
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-TOP 24100 Small Patient ECC Pack Material:701050175R02
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 52301 ¿ Sash & Accessory Pack Material:-709000266R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 30914 ECC Pump Pack 1/4" Material: 709000011
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-TOP 5210 ECC Set - Respiratory Material: 701055604R01
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 30901 CUSTOM CPB PACK Material:701063071
Maquet Cardiovascular, LLC
Maquet Getinge BEQ-TOP 40010 OPEN HEART PACK Material: -701067364R02
Maquet Cardiovascular, LLC
Maquet Getinge-T 8028 PRESSURE PIGTAIL 4" Material: 701055993
Maquet Cardiovascular, LLC
Maquet Getinge-BO-T 41301 BUMC ECC PACK Material: 701065209
Maquet Cardiovascular, LLC
Maquet Getinge-T 41303 AV MANIFOLD FOR ECC PA Material:701066551
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 13901 RAPID RESPONSE Material:701054874
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 44200 MAYO PULMONARY P Material: 701064831
Maquet Cardiovascular, LLC
Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 21506 ECC PACK Material:701064505
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 25503 TMC ¿ with BB & QiD Pedi Material:709000473
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 41200 ECC 1/4 PUMP PAC Material: 701063149
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 30901 CUSTOM CPB PACK Material: 701055372
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 8803#Circ Circuit Small Patient Material: 701048539
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 3501 LVAD/ 3/8" Material: 701068008
Maquet Cardiovascular, LLC
Maquet Getinge-BO-T 2302 Pediatric Cardiac Surgery Pack Material: 709000006
Maquet Cardiovascular, LLC
Maquet Getinge- (1) Material: 701055490R01 BEQ-TOP 15801 ¿ inch ECC Pack (2) Material :701055490R02 BEQ-TOP 15801 1/4 in ECC Pack
Maquet Cardiovascular, LLC
Maquet Getinge- (1) Material: 701063255R01 BEQ-TOP 25003 3/8 3/8 up to 7lpm (2) Material: 701063255R02 BEQ-TOP 25003 3/8 3/8 up to 7 lpm
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 31603 CHKD 3/8" ECC Material: 709000516
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 47800 STRINGFELLOW PED Material:701066583
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 22702 ECC W/HMOD 30000 Material: 701051179
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 28906 1/4" with Bridge Ancillary P Material: 709000072
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 15704 Circulatory Circuit 3/8" Material:701050859R01
Maquet Cardiovascular, LLC
SOLOPATH Re-Collapsible Access System, Model Numbers SR-1925, SR-1935, SR-2025, SR-2035, SR-2225, SR-2235, SR-2425, SR-2435
Terumo Medical Corporation
ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, SKU: a) F00573301020A b) F00573301026X c) F00573301009B Product Usage: ThermaCare(R) HeatWraps…
PF Consumer Healthcare 1 LLC
Maquet Getinge-BEQ-T 9409 Lurie Chlds Large 3/8 Material: 709000428
Maquet Cardiovascular, LLC
Maquet Getinge: (1) Material: 701053941R01 BEQ-TOP 9005 3/8 Custom Pk w/RF32 & HMOD (2) Material: 701053941R02- BEQ-TOP 9005 3/8 Custom Pk w RF32…
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 27602 709000417 Adult Custom Pack Material: 709000417
Maquet Cardiovascular, LLC
Maquet Getinge-T 8029 PRESSURE PIGTAIL 6" Material: 701055995
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 36504 ADULT ECC PACK Material: 701065765
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 8025 1/4" ECC Pack with RF32 Material:701055142
Maquet Cardiovascular, LLC
Fenestrated Tap Adapter (REF# 5001-90011) Product Usage: The K2M Fenestrated Tap System is intended for use as a standalone biopsy tool to remove…
K2M, Inc
Maquet Getinge-BO-T 44201 MAYO PULMONARY PACK Material: 701064834
Maquet Cardiovascular, LLC
Maquet Getinge- BEQ-TOP 32100 Adult Custom Pack Material:701054438R01
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 30300 Material:701052623
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-TOP 30907 ECC PUMP PACK Material: 701065770
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 20705 SMALL PATIENT 1/4 Material: 701053486R01
Maquet Cardiovascular, LLC
Maquet Getinge-BO-TOP 35503 SGD PACK Material: 701067668
Maquet Cardiovascular, LLC
Maquet Getinge-BEQ-T 4903 Mercy Med w/o Oxy Material:701066664
Maquet Cardiovascular, LLC
RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0
Teleflex Medical
Maquet Getinge-BEQ-T 52301 ¿ Sash & Accessory Pack Material: 709000266
Maquet Cardiovascular, LLC
V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, contra-angle, Item Number 502015637
Zimmer GmbH
Drill, contra-angle, 1.5x85mm, Item Number ST502015706
Zimmer GmbH
Nearby Agencies
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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.