Medical device recalls
8 recalls published in the last 7 days. Food, medicines, medical devices, meat and poultry, consumer products and vehicles – 547 recalls since Aug 17, 2026, each with the lot codes, dates and model numbers exactly as the agency lists them.
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Latest recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Aug 26, 2026 |  Siemens Healthcare Diagnostics recall: Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL and 1 more productMedical devices · 20 units; 55 units | Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quini… Serious | FDA Class II |
| Aug 26, 2026 | American Contract Systems recall: Medical procedure kits and trays labeled as: 1) CRANI PACK and 1 more productMedical devices · 4789 kits; 160 kits | a sterility problem Serious | FDA Class II |
| Aug 26, 2026 | AVID Medical recall: Halyard LAVH PACKMedical devices · 40 packs | The kit component was subjected to EO sterilization, contrary to the manufacturer recommen… Serious | FDA Class II |
| Aug 26, 2026 | Boston Scientific recall: OverStitch Suture Cinch and 1 more productMedical devices · 60,654 units | Device may fail to deploy the cinch implant and/or fail to cut the suture as intended. Serious | FDA Class II |
| Aug 26, 2026 | Intersurgical recall: One-Piece Guedel AirwayMedical devices · 21,269 units; 1,575 units | Devices could potentially be occluded or partially occluded. Serious | FDA Class II |
| Aug 26, 2026 | Paragon 28 recall: Custom Made Device Implant 6123 Navicular Cage Small Right Rev A and 1 more productMedical devices · 1; 1 unit | Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elev… Lower risk | FDA Class III |
| Aug 19, 2026 | Baxter Healthcare recall: Baxter Duo-Vent Solution Set and Male Luer Lock AdapterMedical devices · 24528 units | Baxter received customer reports of air bubbles in the drip chamber and tubing when a pres… Most serious | FDA Class I |
| Aug 19, 2026 | Spectra Medical Devices recall: Sodium Chloride InjectionMedical devices · TBD | foreign material Most serious | FDA Class I |
| Aug 19, 2026 | Philips Medical Systems Nederland B.v recall: Philips Azurion RystemMedical devices · 10872 units | Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality … Serious | FDA Class II |
| Aug 19, 2026 | BioFire Diagnostics recall: BIOFIRE Respiratory Panel 2.1Medical devices · 2,370 pouches (79 kits) | Due to increase in false negative results Serious | FDA Class II |
| Aug 19, 2026 | OBP Medical recall: ER-Spec Single-Use Vaginal Speculum with LED Light SourceMedical devices · 8,224 boxes (148,032 units) | There is a potential for vaginal speculums to contain a burr on the proximal plastic blade… Serious | FDA Class II |
| Aug 19, 2026 | Bioporto Diagnostics A/S recall: ProNephro AKIMedical devices · 400 units | The use of a non-validated rework process for assay reagents which could lead to missed di… Serious | FDA Class II |
| Aug 19, 2026 | Straumann recall: GM Helix ImplantMedical devices · 417 US | There may be a mismatch between the implant contained inside the packaging and the informa… Serious | FDA Class II |
| Aug 19, 2026 | Waldemar Link GmbH & Co. KG recall: Endo-ModelMedical devices · 1 US; 9 OUS | The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly co… Serious | FDA Class II |
| Aug 19, 2026 | BD Switzerland Sarl recall: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext…Medical devices · 93,700 | Products may not have received adequate sterilization processing. Serious | FDA Class II |
| Aug 19, 2026 | Spacelabs Healthcare recall: Xhibit Central StationMedical devices · 6074 | Due to off-the-shelf display port component that has audio/video failures Serious | FDA Class II |
| Aug 19, 2026 | Straumann recall: Bone Level TaperedMedical devices · 175 units | Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadverten… Serious | FDA Class II |
| Aug 19, 2026 | Erbe recall: ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000Medical devices · 1126 units | A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumati… Serious | FDA Class II |
| Aug 19, 2026 | Philips Medical Systems Nederland B.v recall: Philips AzurionMedical devices · 2016 units | Two software related issues: 1) Potential image quality degradation that may lead to delay… Serious | FDA Class II |
| Aug 19, 2026 | Remel Europe recall: Thermo Fisher Diagnostics Neisseria meningitidis Gp CMedical devices · 26 units | Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU c… Serious | FDA Class II |
| Aug 19, 2026 | Ventana Medical Systems recall: Navify Digital PathologyMedical devices · 190 | Due to complaints received for the Image Management System regarding image/metadata discre… Serious | FDA Class II |
| Aug 19, 2026 | Galt Medical recall: Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MPMedical devices · 114,260 kits | Black depth markings may detach from the outer sheath of the coaxial dilator introducer co… Serious | FDA Class II |
| Aug 19, 2026 | Terumo Medical recall: Glidesheath Slender a-Kit 6F 10CM .021GWMedical devices · 7,490 units | Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. Serious | FDA Class II |
| Aug 19, 2026 | Philips Medical Systems Nederland B.v recall: Allura Xper FDMedical devices · 4,252 units | Firmware issue potentially leading to loss of geometry movements. Serious | FDA Class II |
| Aug 19, 2026 | Medline Industries recall: Medline Micro-Kill Bleach Germicidal Bleach WipesMedical devices · 591,561 units; 447,618 units; 1,244 units; 31,728 | Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concen… Serious | FDA Class II |
| Aug 19, 2026 | Microvention recall: BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US…Medical devices · 5500 devices | Due to an increase rate of balloon pinhole defects. Serious | FDA Class II |
| Aug 19, 2026 | Covidien recall: V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22… and 4 more productsMedical devices · 135,875 total | Product may contain a perforation or tear in the sterile barrier packaging. This issue may… Serious | FDA Class II |
| Aug 19, 2026 | Cardinal Health 200 recall: Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT and 7 more productsMedical devices · 36862 kits; 456 kits; 80 kits; 87182 kits; 602 kits; 401311 kits; 52699 kits; 616 kits | Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexp… Serious | FDA Class II |
| Aug 19, 2026 | W L Gore & Associates recall: GORE VIABIL Short Wire Biliary EndoprosthesisMedical devices · 13 units | 10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10… Serious | FDA Class II |
Recalls by brand
How to read a recall
Identifiers decide whether your product is included. A recall almost never covers every package with a brand name: it lists lot codes, UPC barcodes, best-by or use-by dates, establishment numbers (the “EST.” number inside the USDA mark on meat and poultry), model numbers or – for vehicles – model years and build dates. Compare them with what you have before you throw anything away.
Which agency: the FDA covers most food, medicines, supplements, cosmetics and medical devices; USDA's Food Safety and Inspection Service covers meat, poultry and processed egg products; the CPSC covers consumer products from toys to appliances; NHTSA covers vehicles, tires, child car seats and motor-vehicle equipment. FDA enforcement reports appear weekly and can list a recall several weeks after the company first announced it.
Recall questions
What products were recalled this week?
8 recalls were published by the FDA, USDA, CPSC and NHTSA in the last 7 days, 0 of them in the most serious category: 6 consumer products, 2 vehicles. The newest: Siemens Healthcare Diagnostics recall: Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL and 1 more product (Aug 26, 2026).
How do I know if a product I bought is recalled?
Search this page by brand or product name, then compare the lot code, UPC, best-by date or model number on your package with the identifiers on the recall page – a recall usually covers only certain lots or dates, not every product with that name. For a car, enter your 17-character VIN at nhtsa.gov/recalls.
What does Class I recall mean?
The FDA and USDA rate recalls by risk. Class I is the most serious: a reasonable probability that the product will cause serious health problems or death. Class II may cause temporary or reversible health problems; Class III is unlikely to cause harm.
Do I get my money back for a recalled product?
Usually yes. Food recalls ask you to throw the product away or return it to the store for a refund; CPSC recalls offer a free refund, repair or replacement; vehicle safety recalls are repaired free at a dealer. Each recall page shows the remedy the agency lists.
Recalls by type
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.