PlainRecalls
2023 data Federal recall API Linked to agency record

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

39,794 recalls · Page 160 of 796

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FDA Medical Devices Recall Insight

According to PlainRecalls' agency ranking (distinct recall events, same sort as /agency), FDA Medical Devices sits #1 of 6 (1st among 6 issuing agencies) with 39,794 notices, about 38.1% of the 104,423-record archive. 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 796 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 2 critical (Class I-equivalent) actions, 48 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 33 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 Feb 7, 2024 to Feb 7, 2024, covering 11 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).

Moderate Feb 7, 2024

DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A

MEDLINE INDUSTRIES, LP - Northfield

Moderate Feb 7, 2024

HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-28J

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Achieva XR. Model (REF) Numbers 781153, 781253.

Philips North America

Moderate Feb 7, 2024

P7 28MM 10 DEGREE +4MM INSERT Intended for knee replacement Part Number: 6302-6-107

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST), ECHELON Endopath Stapler, Endoscopic Linear Cutter Reload (+Gripping Surface technology), 45MM WHITE VASCULAR/THIN, Product No. GST45W

Ethicon Endo-Surgery Inc

Moderate Feb 7, 2024

RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-931

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number: 3052-0524

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7521

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-228

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- Intended for knee replacement Part Number: 72-15-0324

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

LEFT X-LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-328

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

P7 32MM 1O DEGREE +4MM INSERT Intended for knee replacement Part Number: 6302-6-307

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model: BD-400P-1080

Olympus Corporation of the Americas

Moderate Feb 7, 2024

MEDLINE ADULT BLOOD CULTURE KIT, Reorder Number DYNDH1694A

MEDLINE INDUSTRIES, LP - Northfield

Moderate Feb 7, 2024

NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL

THOR Photomedicine Ltd

Moderate Feb 7, 2024

MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";

Aesculap Inc

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) Baby PICC Kit, kit number UIBP90J; b) Baby PICC Kit, kit number UIBP90K; c) PORT PACK (PS 058330), kit number UIPO82AB; d) Pediatric PICC Kit, kit number UIPP76K;

American Contract Systems, Inc.

Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-2110

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Achieva 1.5T Initial system. Model (REF) Numbers 781178.

Philips North America

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LOWER PELVIC PACK, kit number AGLP52L; b) OB/GYN DAVINCI PACK A RG BASIN, kit number HGOB98G; c) DAVINCI GYN PACK, kit number HHDV17; d) KIT, GYNE ROBOTIC, kit number MMGR44D; e) KIT, MAJOR LITHOTOMY, kit number MMJL16E; f) GYN PACK, kit number SMGY46; g) Lithotomy Pack, kit number THLH71C; h) ASC HYSTEROSCOPY PACK (PS 020634), kit number UIHY16AA; i) GYN LAPAROSCOPY HPES, kit number

American Contract Systems, Inc.

Moderate Feb 7, 2024

DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2-200

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

SCORPIO TS TIB INSERT-Intended for knee replacement Part Number:72-4-7512

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7524

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco Dental Chemical Integrator [5726-583] Tuttnauer (WTL198-0082) Terragene Integron (PCD26-C) Terragene Bionova PCD (PCD222-C)

TERRAGENE S.A.

Moderate Feb 7, 2024

RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-928

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) C-SECTION PACK, kit number FDCS01AA; b) C-SECTION PACK, kit number FDCS01AB; c) C-SECTION STERILE PACK, kit number HGCS68J; d) C-SECTION PACK, kit number HICS50H; e) C-SECTION PPS, kit number LLCI66; f) C-Section drape Pack, kit number RBCS12R; g) C-Section, kit number THCS49B; h) C-SECTION PACK (PS 020632), kit number UICS50AG;

American Contract Systems, Inc.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, cardiac, labeled as: a) HEART CATHETERIZATION TRAY, kit number JRHC45G; b) TAVR PACK, kit number LLTV10; c) CATH PED LF SJH, kit number SJCA21F; d) CATH HEART ADL LF SJH, kit number SJCH22F; e) INT RAD PORTS-LF - 206060, kit number UDIR58AL

American Contract Systems, Inc.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) IR NEURO PACK, kit number AGNE20J; b) ADULT CRANIOTOMY PACK, kit number LLCR99; c) LAMINECTOMY PACK, kit number LLLC26; d) KIT, CRANIOTOMY, kit number MMCR11J; e) KIT, NEURO SPINE, kit number MMNS20H; f) IR NEURO PACK, kit number OSIN77; g) NEURO SAH, kit number SANE32H; h) NEURO SAH, kit number SANE32I; i) S78FCH CRANI PACK (PS 132432), kit number UICR10U; j) CRANI PACK (PS039498), kit number

American Contract Systems, Inc.

Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE TRAY ADULT, Reorder Number DYNDH1194A

MEDLINE INDUSTRIES, LP - Northfield

Moderate Feb 7, 2024

Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.

Philips North America

Moderate Feb 7, 2024

DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-709

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.

Philips North America

Moderate Feb 7, 2024

Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.

Philips North America

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, gastroenterological & urological, labeled as: AHN BIOPSY STERILE, kit number AHBP12A

American Contract Systems, Inc.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general & plastic surgery, labeled as: a) Breast Plastics Pack, kit number BBPL20D; b) MINOR PLASTIC, kit number WPMP16H

American Contract Systems, Inc.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LABOR & DELIVERY PACK, kit number HILD52F; b) LABOR & DELIVERY PACK, kit number HILD52G

American Contract Systems, Inc.

Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-1555

Olympus Corporation of the Americas

Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, urological, labeled as: a) UROLOGY DAVINCI PACK, kit number HGUR87G; b) CYSTO PACK, kit number LVCY20; c) URO ROBOTIC PACK, kit number LVUR44;

American Contract Systems, Inc.

Moderate Feb 7, 2024

Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.

Philips North America

Critical Feb 7, 2024

EvAir CPRSR Kit Upgrade: a) DISS/CEE 7/7 230V 50/60 HZ, Model Number M1230849; b) DISS/NEMA 5-15 115V 60 HZ, Model Number M1230847; c) NIST/BS 1363 230V 50/60 HZ, Model Number M1230849; d) NIST/BS 546 230V 50/60 HZ, Model Number M1230849; e) NIST/CEE 7/7 230V 50/60 HZ, Model Number M1230849;

Datex-Ohmeda, Inc.

Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3910

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0910

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

Sofsilk Braided Silk sutures: CS-211 SOFSILK* 4-0 BLK 45CM CVF21 X36 GS-831 SOFSILK* 4-0 BLK 75CM V20 X36 S-176 SOFSILK* 0 BLK 12X45CM PCT X24 S-182 SOFSILK* 5-0 BLK 12X45CM PCT X36 S-184 SOFSILK* 3-0 BLK 12X45CM PCT X36 S-185 SOFSILK* 2-0 BLK 12X45CM PCT X36 S-245 SOFSILK* 2-0 BLK 12X60CM PCT X36 S-246 SOFSILK* 0 BLK 6X60CM PCT X36 S-2782K SOFSILK* 4-0 WHI 45CM SS24 DA S-303 SOFSILK* 4-0 BLK 12X75CM PCT X36 S-304 SOFSILK* 3-0 BLK 12X75CM PCT X36 S-305 SOFSILK* 2-0 BLK 12X75CM PCT X36 S-316 SOF

Covidien LP

Moderate Feb 7, 2024

RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-831

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-231

Howmedica Osteonics Corp.

Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-2055

Olympus Corporation of the Americas

Critical Feb 7, 2024

EVair air compressor, model numbers: M1230849 and M1230847

Datex-Ohmeda, Inc.

Moderate Feb 7, 2024

Custom procedural convenience kits and trays, anesthesia, labeled as: a) HEART ANESTHESIA BUNDLE NS, Kit Number LMHA01V; b) OR/Anesthesia Central Line Insertion Kit, Kit Number UIAN43L

American Contract Systems, Inc.

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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.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS 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 September 2026.