State
20,188 recalls have nationwide distribution and so reach New York. 0 additional recalls listed New York specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect New York consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Some bottles of Acetaminophen Extra Strength 500 mg tablets are labeled with the drug facts information for Aspirin 81 mg tablets. The affected lot is 4138197 (expiration 10/31/2025), distributed nationwide.
Medline procedure kits containing defective plastic syringes have been recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects over 1.6 million units distributed worldwide.
Palmer & Company is recalling Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists and Palmer Candy Frosted Patriotic Pretzels nationwide due to potential salmonella contamination.
Palmer & Company is recalling Sunny Select Strawberry Yogurt Coated Pretzels (10 oz, UPC 9848796055) distributed nationwide in the US and Canada due to potential salmonella contamination.
Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.
Umary Acido Hialuronico dietary supplement (850 mg caplets) was recalled nationwide by the FDA for containing undeclared Diclofenac and Omeprazole. The product was marketed without an approved drug application.
Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.
Palmer & Company is recalling Palmer Candy Cookies & Cream Yummy Chow (Item 10706) nationwide due to potential salmonella contamination. Consumers should not consume the product.
Palmer & Company is recalling Urge! Caramel Swirl Pretzels and Casey's Caramel Swirl Coated Pretzels nationwide due to potential Salmonella contamination.
Palmer & Company is recalling Palmer Frosted Munchy Medley snack mix nationwide (US and Canada) due to potential salmonella contamination. Consumers should not eat the product and should discard it or return it to where purchased.
Palmer & Company is recalling Palmer Zebra Fudge Cookies due to potential salmonella contamination. The product was distributed nationwide in the United States and Canada.
Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.
Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.
Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.
Luminex recalls approximately 1,100 diagnostic kits due to defective test cartridges that may produce false positive results for Staphylococcus lugdunensis and Enterococcus faecium bacteria.
Baxter Healthcare Corporation is recalling the PST 500 U Precision Surgical Table due to loose spring pins that can cause the tabletop to unexpectedly tilt or move, potentially causing unintended patient movement during surgery.
CareFusion is recalling BD PYXIS MEDBANK medication dispensing cabinets due to a software issue that causes incorrect bin information to print on restock labels, potentially leading to medication selection errors.
A software defect in BD PYXIS MEDBANK automated medication dispensing cabinets may cause the incorrect medication bin to be printed on restock labels, potentially resulting in medication errors.
A software issue in the BD PYXIS MDBNK medication dispensing cabinet may cause restock labels to print with incorrect bin locations, potentially affecting medication storage accuracy.
Siemens LUMINOS Lotus Max X-ray displays are being recalled because the support arm may lower unintentionally, potentially injuring people nearby during positioning.
CareFusion's BD PYXIS MEDBANK medication dispensing cabinets (software 3.9.1.9) have a software defect that may cause restock labels to print incorrect medication bin locations, creating a risk of medication dispensing errors.
The support arm on Siemens Multitom Rax X-ray systems may unintentionally lower, creating a fall risk to people positioned beneath the ceiling-mounted display during system positioning.
A software issue in BD PYXIS MEDBANK automated medication dispensing cabinets can cause incorrect medication bin labels on restock labels, potentially leading to medication storage errors.
The FDA is recalling 180 Leica HistoCore Arcadia H paraffin embedding stations due to a sealing defect in the paraffin tank that can cause toxic smoke and internal fire.
Steris Hookup Model 2-8-540 instructions were incorrectly documented, potentially preventing proper endoscope disinfection and risking patient infection.