New York recalls

Medline's IV Start Convenience Kits contain sterile applicators (BD ChloraPrep Clear and FREPP Clear) with wrinkles in the paper packaging that may compromise the sterile barrier. If the seal is breached, patients could be exposed to microbial contamination during IV insertion or blood draws.

Medline's Arterial Line Insertion Kit (Model ART1295) contains sterilization applicators with wrinkles in the paper packaging that may compromise the sterile barrier. If the seal is breached, patients could be exposed to microbial contamination, ranging from no effect to serious infection.

Several Medline medical convenience kits—including IV start kits, blood culture kits, and pediatric emergency trays—contain sterile applicators with wrinkles in the packaging that may compromise the sterile barrier. If the packaging is damaged, the contents could be exposed to microbial contamination, which could cause infection ranging from minor to serious.

Medline's Ultrasound Breast Pack (Model DYNJ63375C) contains sterilized applicators with wrinkles in the paper packaging that may compromise the sterile barrier. If the packaging is damaged, the applicators could be exposed to microbial contamination before use.

Medline Convenience Kits (Model DYNJ906437D) containing BD ChloraPrep and FREPP applicators have wrinkles in the paper packaging that may compromise the sterile barrier. If the packaging is breached, patients could be exposed to microbial contamination.

Medline's IVS Blood Culture Kits (models DYNDH1920 and DYNDH1920A) contain sterile applicators with wrinkles in the paper packaging that may compromise the sterile barrier. If the seal is breached, the applicators could be exposed to microbial contamination before use.

Medline Convenience Kits containing BD ChloraPrep Clear and FREPP Clear applicators may have packaging defects—wrinkles in the paper lid that could compromise the sterile barrier. If the packaging is compromised, the sterile applicators inside could be exposed to microbial contamination before use.

Several Medline Convenience Kits contain BD ChloraPrep Clear and FREPP Clear applicators with wrinkled paper packaging that may compromise the sterile barrier. If the packaging is breached, the applicators could be exposed to microbial contamination, which could lead to localized or serious infection in patients.

Two Medline Convenience Kits contain BD ChloraPrep Clear applicators with wrinkles in the paper packaging that may compromise the sterile barrier. If the sterile seal is breached, the applicators could be contaminated with microbes, potentially exposing patients and users to infection.

Diagnostica Stago identified a positive drift in quality control (QC) values in one lot of STA Staclot Protein S reagent within the product's stated 4-hour stability period. This drift could affect the accuracy of test results performed during that window. The issue affects reagent Lot 273074 distributed nationwide.

Halyard medical convenience kits contain Ritmed Neurological Sponges that may have unexpected variability in endotoxin levels. Endotoxins are bacterial substances that can trigger immune reactions in patients. The affected kits were distributed nationwide to surgical facilities.

AVID Medical is recalling 70 different neurological and spine surgical kits that contain Ritmed Neurological Sponges. The sponges may have unexpected variability in endotoxin levels, which could affect their safety and sterility during surgical use.

Halyard medical convenience kits contain Ritmed Neurological Sponges that may have unexpected variability in endotoxin levels. Endotoxins are bacterial substances that could trigger an immune response if present at higher-than-expected levels. About 11,763 kits across multiple surgical specialties are affected.

Philips has identified an unintended radiation issue affecting Philips Brilliance CT 64 CT scanner systems (Software 4.1.10.x) that could impact equipment performance. The issue affects multiple Philips CT system models including IQon, iCT, Ingenuity, and Brilliance CT 64.

Philips has identified an unintended radiation issue affecting Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could impact equipment performance. The issue affects specific software versions and product codes distributed in the US and US territories.

Philips has identified an unintended radiation issue affecting the IQon Spectral CT and related CT systems (iCT, Ingenuity, and Brilliance CT 64 models). This issue could affect the performance of the equipment. The problem was found in software version 4.7.7.x.

Philips has identified an unintended radiation issue affecting Philips Brilliance iCT, Brilliance iCT Upgrades, and Brilliance iCT SP CT scanner systems running software version 4.1.10.x. This issue could affect the performance and safety of the equipment.

Fayus Inc. recalled OLA-OLA Pounded Yam (Iyan) products in 2 lb, 4 lb, 5 lb, and 10 lb bags because some packages contain undeclared milk. The product was mislabeled during packaging for different markets. This poses a serious risk to people with milk allergies or sensitivities.

Wonton Specialist Inc. cooked noodles (16 oz and 5 lb bags) contain FD&C Red No. 40, a food dye that is not declared on the label. The product was distributed in New York, New Jersey, and Pennsylvania. No injuries have been reported.

Wonton Specialist Inc. dumpling skin (16 oz packages) contains FD&C Red No. 40 food dye that is not listed on the label. The product was distributed in New York, New Jersey, and Pennsylvania. About 240 bags are affected.

Wonton Specialist Inc. wonton skins (16 oz packages) contain FD&C Red No. 40, a food dye that was not declared on the label. This poses a risk to people with allergies or sensitivities to this dye. About 480 bags were distributed in New York, New Jersey, and Pennsylvania.

Wonton Specialist Inc. is recalling 16 oz packages of Lo Mein Noodle because they contain FD&C Red No. 40 (a food dye) that is not listed on the label. This can be a concern for people with allergies or sensitivities to this ingredient or those who avoid it for dietary or religious reasons.

Wonton Specialist Inc. noodles (12 oz and 5 lb packages) contain FD&C Red No. 40 food dye that is not listed on the label. This undeclared ingredient may pose a risk to people with allergies or sensitivities to the dye. About 550 bags are affected.

Wonton Specialist Inc. pan fried noodles in 16 oz and 5 lb bags contain FD&C Red No. 40, a food dye that is not declared on the label. This poses a risk to people with allergies or sensitivities to artificial dyes, and to those who avoid the ingredient for religious or personal reasons. About 500 bags were distributed in New York, New Jersey, and Pennsylvania.

Savor Seasonings LLC's bulk Organic Cheddar Type Seasoning tested positive for milk allergen that was not listed on the label. The affected product is packaged in 50-lb bags and distributed in Canada. This poses a serious risk to people with milk allergies.

The Hampton Grocer's Lacnola Small Batch Lactation Granola (8 oz pouches) may be contaminated with Salmonella. Two specific lot codes are affected: HGLC-102125 (expires 21 Oct 2026) and HGLC-021326 (expires 13 Feb 2027).

Prince Bakery Inc. is recalling Prince Sesame French Bread because sesame is not listed in the ingredient statement, even though the product name indicates it contains sesame. People with sesame allergies could have a serious reaction if they eat this bread without knowing sesame is present.

Prince Bakery Italian Bread labeled as containing sesame does not list sesame in its ingredient statement. People with sesame allergies relying on the ingredient list may not realize the product contains sesame, which they need to avoid.

Optimal Balance Pharmacy's Glutathione 200 mg/mL injectable solution failed quality testing and was found to contain bacterial endotoxin levels above safe limits. This contamination poses a risk of serious infection or systemic reaction when injected. The affected lot (LG342009076) was distributed nationwide.

Baxter Healthcare Corporation is recalling 0.9% Sodium Chloride Injection USP in 500 mL VIAFLEX plastic containers because some bags contain fiberglass particles. The affected lots are Y495523 and Y495523A, expiring October 31, 2027. No injuries have been reported.