New York recalls
4,074 federal recalls affecting New York in the last 12 months - 420 New York-specific plus 3,654 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-09-09FDA-DeviceFresenius Medical CareClass IINationwideFresenius dialysis tubing set recalled for blood leak risk
Fresenius Medical Care is recalling specific lots of the 5008X HD/HDF Twister Blood Tubing Set (Part Number 03-5350-8) because the connection between the Arterial Alpha Clip and the main line may leak during dialysis treatment. A leak could result in blood loss and low blood volume.
- 2026-09-09FDA-DeviceFresenius Medical CareClass IINationwideFresenius dialysis tubing set recalled for blood leak risk
Fresenius Medical Care is recalling certain 5008X HD/HDF blood tubing sets (part number 03-5300-3C) due to a heightened risk of blood leaks at the connection between the Arterial Alpha Clip and the main line. Blood leaks during dialysis treatment can result in significant blood loss.
- 2026-09-09FDA-DeviceFresenius Medical CareClass IINationwideFresenius blood tubing set recalled for blood leak risk
Fresenius Medical Care is recalling certain 5008X HD/HDF Standard Blood Tubing Sets due to a heightened risk of blood leaking from the connection between the Arterial Alpha Clip and the main line or pump segment. A blood leak during dialysis treatment could result in blood loss and low blood volume.
- 2026-09-09FDA-DeviceFresenius Medical CareClass IINationwideFresenius blood tubing set recalled for leak risk
Fresenius Medical Care is recalling certain 5008X Standard HD Pre-Flush blood tubing sets due to a heightened risk of blood leaking from the connection between the Arterial Alpha Clip and the main line. A leak during dialysis treatment could result in blood loss.
- 2026-09-09FDA-DeviceBoston ScientificClass IINationwideBoston Scientific cardiac monitor recalled for delayed alert notifications
Boston Scientific's server software for LUX-Dx insertable cardiac monitors may delay notifications of atrial fibrillation (AF) burden alerts. This delay could postpone a doctor's evaluation or treatment of an irregular heart rhythm.
- 2026-09-09FDA-DeviceBoston ScientificClass IINationwideBoston Scientific LUX-Dx cardiac monitor alert delay risk
Boston Scientific's LUX-Dx, LUX-Dx II, and LUX-Dx II+ insertable cardiac monitors may experience delays in sending AF Burden Alert notifications through their server software. These delayed alerts could postpone a patient's medical evaluation or treatment for irregular heart rhythms.
- 2026-09-09FDA-DeviceBoston ScientificClass IINationwideBoston Scientific LUX-Dx cardiac monitor recalled for delayed alerts
Boston Scientific's server software that supports LUX-Dx, LUX-Dx II, and LUX-Dx II+ insertable cardiac monitors may delay notifications of abnormal heart rhythm (atrial fibrillation) alerts. This delay could postpone a patient's clinical evaluation or treatment of an irregular heartbeat.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for defective ChloraPrep applicator seals
Medline Convenience Kits containing BD ChloraPrep Clear applicators (Ortho Aspiration Kit DYKM1636A, Lot 26EBI940) may have packaging with open or incomplete seals. If a sealed applicator is compromised, it could allow contamination that may cause localized or systemic infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Cataract Preop Kits recalled for defective applicator seals
Medline Convenience Kits (model DYKS1583A) contain BD ChloraPrep Clear applicators from specific lots with open or incomplete seals on the packaging. A sealed applicator that has been compromised may allow contamination, which could lead to infection if used during surgery.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for contaminated ChloraPrep applicators
Medline Convenience Kits containing BD ChloraPrep Clear 1mL applicators from specific lots may have open or incomplete seals on the applicator packaging. These applicators are used for skin prep before cesarean sections. Contaminated applicators could lead to skin, soft tissue, or systemic infections.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for ChloraPrep applicator seal defect
Medline Convenience Kits containing BD ChloraPrep Clear applicators from specific lots may have open or incomplete seals on the applicator packaging. If a seal is compromised, the applicator could become contaminated and cause skin, soft tissue, or systemic infection if used.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for defective ChloraPrep applicators
Medline Convenience Kits contain BD ChloraPrep Clear applicators from certain lots with defective or incomplete seals on the packaging. If an applicator seal is compromised, the applicator may be contaminated, which could lead to skin, soft tissue, or systemic infection if used.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline pre-op kits recalled for defective ChloraPrep applicators
Medline Convenience Kits containing BD ChloraPrep Clear applicators from specific lots may have open or incomplete seals on the applicator packaging. Using a potentially contaminated applicator could lead to skin, soft tissue, or systemic infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline blood culture kits recalled for contaminated applicators
Medline Convenience Kits containing BD ChloraPrep Clear applicators from specific product lots may have open or incomplete seals on the applicator packaging. These kits are used in healthcare settings for blood draws and culture collection. Contaminated applicators could potentially lead to skin, soft tissue, or systemic infections.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for ChloraPrep applicator seal defect
Medline Convenience Kits containing BD ChloraPrep Clear 1mL applicators from specific lots may have open or incomplete seals on the applicator packaging. If a contaminated applicator is used for blood culture collection or skin prep, it could cause localized skin infection, soft tissue infection, or more serious systemic infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline IV Start Kits recalled for contaminated applicators
Medline Convenience Kits containing BD ChloraPrep Clear applicators from specific lots may have open or incomplete seals on the applicator packaging. Use of a potentially contaminated applicator during IV insertion or lab draws could lead to skin, soft tissue, or systemic infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for contaminated applicators
Medline Convenience Kits containing BD ChloraPrep Clear 1mL applicators from specific lots are being recalled because the applicator packaging may have an open or incomplete seal. If the sealed applicator is compromised, it could become contaminated and lead to skin, soft tissue, or systemic infections when used.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for open applicator seals
Medline Industries is recalling specific lots of Convenience Kits that contain BD ChloraPrep Clear applicators. The applicator packaging may have an open or incomplete seal, which could allow contamination. If a contaminated applicator is used, it may cause skin, soft tissue, or systemic infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for ChloraPrep applicator seal defects
Medline Convenience Kits containing BD ChloraPrep Clear 1mL applicators from specific lots may have open or incomplete seals on the applicator packaging. This could allow contamination, potentially leading to skin, soft tissue, or systemic infections if used during medical procedures.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for contaminated ChloraPrep applicators
Medline Convenience Kits (Pain Pre Op Kit, model DYKS1476A) contain BD ChloraPrep Clear applicators from specific lots with potentially open or incomplete seals. The compromised packaging may allow contamination of the applicator, which could lead to skin, soft tissue, or systemic infection if used.
- 2026-09-09FDA-DeviceBaxterClass IINationwideBaxter Novum IQ Syringe Pump recalled for software glitch
A software issue in the Baxter Novum IQ Syringe Pump (Model 40800BAXUSL) may occur when you replace an empty syringe during a multi-syringe infusion while medication still needs to be delivered. This could affect the accuracy of drug delivery. Four loaner units have been identified and are affected.
- 2026-09-09FDA-DeviceBaxterClass IINationwideBaxter Novum IQ Syringe Pump recalled for software issue
A software problem in the Baxter Novum IQ Syringe Pump (Model 40800BAXUS) can occur when a syringe empties and is replaced during a multi-syringe infusion, potentially affecting the accuracy of medication delivery. The issue affects about 14,601 units distributed nationwide.
- 2026-09-09FDA-DeviceJohnson & Johnson Surgical VisionClass IINationwideHEALON EndoCoat PRO and DUET PRO II need updated surgical instructions
Johnson & Johnson is sending updated surgical instructions for HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products used in cataract surgery. The new instructions emphasize that if resistance is felt when inserting the cannula, surgeons should stop, withdraw the cannula, and reassess insertion conditions rather than forcing it—to avoid potential injury to the cornea, iris, or Descemet's membrane (a delicate eye structure).
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline phlebotomy and blood culture kits recalled for contamination risk
Medline's blood draw and phlebotomy kits contain antiseptic applicators (BD ChloraPrep Clear and FREPP Clear) with wrinkles in the paper packaging that may compromise the sterile barrier. If the packaging is damaged, the applicators could be exposed to bacterial or microbial contamination before use.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for contamination risk
Medline's Ortho Aspiration, Should Block, and Trima Convenience Kits contain sterile applicators with wrinkles in the paper packaging that may compromise the sterile seal. If the sterile barrier is breached, patients could be exposed to microbial contamination, potentially causing localized or serious infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for sterility packaging defect
Medline Convenience Kits (Eye Kit and Cataract Preop Kit models) contain sterilized applicators with a potential packaging defect—wrinkles in the paper lidding that may compromise the sterile barrier. If the packaging is breached, patients could be exposed to microbial contamination, ranging from no injury to infection.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline C-Section Prep kits recalled for sterility packaging breach
Medline's C-Section Prep Convenience Kits contain ChloraPrep and FREPP applicators with a potential sterility packaging breach due to wrinkles in the paper lid seal. If the sterile barrier is compromised, users may be exposed to microbial contamination. Health effects could range from no injury to localized infection, or in rare cases, serious infection requiring treatment or hospitalization.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline Convenience Kits recalled for sterility breach risk
Medline's Labor CDS and Vaginal Delivery Admission Bag kits contain ChloraPrep and FREPP applicators with wrinkled packaging that may compromise the sterile barrier. If the seal is breached, patients and healthcare workers may be exposed to microbial contamination, ranging from no injury to serious infection requiring treatment.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline pre-op surgical kits recalled for sterility risk
Medline pre-op and cataract surgery kits containing BD ChloraPrep Clear applicators may have compromised sterile packaging due to wrinkles in the paper lidding. If the sterile barrier is breached, patients could be exposed to microbial contamination during surgery.
- 2026-09-09FDA-DeviceMedlineClass IINationwideMedline blood culture kits recalled for contamination risk
Medline's blood culture convenience kits contain sterile applicators with a potential packaging defect—wrinkles in the paper lidding may compromise the sterile barrier. If the seal is breached, the applicators could be exposed to microbial contamination, which could potentially cause infection if used.
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