Product category · Updated Jun 3, 2026
Medical Devices recalls
Medical device recalls including implants, diagnostic equipment, and surgical tools
Medical Devices accounts for 40,478 recalls — about 40.4% of the federal recall archive, of which 9% of graded records are high-severity.
The FDA, CPSC and NHTSA have published 40,478 medical devices recalls between 2000 and 2026 — roughly 40.4% of the 100,165-record archive. Of the 40,478 records graded for severity, 9% are high-severity. Most are issued by FDA Devices. Counts reflect market size and reporting activity, not a product's inherent danger.
- 40,478 total recalls
- 40.4% of the archive
- 9% graded high-severity
- FDA Devices top agency
Category snapshot
Medical Devices accounts for 40,478 recalls — about 40.4% of the 100,165-record federal archive, with 3,549 graded high-severity, most issued by FDA Devices.
- 40,478
- total recalls
- 9%
- graded high-severity
- FDA Devices
- top issuing agency
- 2000–2026
- years covered
Medical Devices recalls by year
2000–2026
Severity distribution
Graded records only
- High severity 3,549
High severity
3,549 recalls
- Moderate
Moderate
35,871 recalls
- Lower severity 1,058
Lower severity
1,058 recalls
Recalls by issuing agency
- FDA Devices
FDA Devices
39,096 recalls
- FDA Drug 882
FDA Drug
882 recalls
- CPSC 441
CPSC
441 recalls
- FDA Food 59
FDA Food
59 recalls
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Recalls in Medical Devices
Newest first · Page 28 of 810
Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P
Medline Industries, LP
Stryker MV3 bariatric bed, Part Number 5900000001
Stryker Medical Division of Stryker Corporation
DEXLOCK Achilles Repair Implant Kits, MAKT4520
Medline Industries, LP
Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee component of limb salvage replacem…
Waldemar Link GmbH & Co. KG (Mfg Site)
MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C
Medline Industries, LP
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Nipro Medical Corporation
Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
Medline Industries, LP
Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-…
Orthofix U.S. LLC
ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the pati…
Draeger, Inc.
Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMP…
Orthofix U.S. LLC
Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23…
Orthofix U.S. LLC
BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
C.R. Bard Inc
IntelliVue MP90. Product Number: M8010A.
Philips North America Llc
Food Intolerance Test Small
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IntelliVue MP30. Product Number: M8002A.
Philips North America Llc
Vitamin D-Test
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Candida Test
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Organic Acids Profile Test Large
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Allergy Test IgE
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Allergy test Small
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IntelliVue Patient Monitor MX800. Product Number: 865240.
Philips North America Llc
GI Microbiome Profile XL
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Illegally Marketed
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HPV Antigen Test
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Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Philips Ultrasound, LLC
Sperm Test
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Mycoplasma test, IgG and IgM
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Parasite Test
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Adrenal Test
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Neurotransmitters Plus
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Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.
Baxter Healthcare Corporation
Pollen Allergy Test
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Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.
Fresenius Kabi USA, LLC
Alcohol (ALC) Test Saliva
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Gut Microbiome Test XL
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Pet Allergy Test
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IntelliVue Patient Monitor MX700. Product Number: 865241.
Philips North America Llc
CT 5300; Software Version Number: 4.5, 5.0, 5.1;
Philips North America Llc
Urinary Tract Infection Test
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IntelliVue Patient Monitor MX500. Product Number: 866064.
Philips North America Llc
Lactose Intolerance Test
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Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
Paragon 28, Inc.
PSA Test
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IntelliVue Patient Monitor MX850. Product Number: 866470.
Philips North America Llc
Gut Microbiome Test Small
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8 in 1 STI Test Kit
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Akkermansia Test
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MAMMOMAT Inspiration;
Siemens Medical Solutions USA, Inc
Food Intolerance Test Medium
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KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Microbiologics Inc
What to do with this
Monitoring medical devices? Start here.
- Check a specific product against the full federal archive before you use or buy it. Recall checker
- Most medical devices recalls come from FDA Devices — browse that agency's full feed. FDA Devices recalls
- Sort the whole archive by severity to see the highest-risk active recalls first. Rankings
Recall categorization follows the issuing agency's product taxonomy; always confirm specifics on the official notice.
Nearby categories
Adjacent product categories that share hazard patterns or regulatory oversight.
Data sources
- Source: FDA — openFDA Enforcement API (food, drug, and device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls
- Source: NHTSA — National Highway Traffic Safety Administration Recalls (vehicles & equipment)
Category data as of Jun 3, 2026.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Category counts and the year trend are computed across the full archive for medical devices. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of Jun 3, 2026.