State

New York product recalls

73,833 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,956
Critical: 1,508
Severe: 3,702
Most recent: 2026-11-04

Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52076–52100 of 86789

HighFDA (Devices)·Z-1740-2017·2017-04-12
Recall of Sterile Eye Pads Due to Compromised Sterility Barrier
Covidien LLC is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility.
Product
Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7 cm), Sterile Item Code: 2841 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1734-2017·2017-04-12
Centurion Medical Recalls Post-Operative Ophthalmic Dressing Kits Due to Sterility Concerns
Centurion Medical Products is recalling 45 post-operative ophthalmic dressing kits because the eye pads inside may have had a breach in sterile packaging.
Product
POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
ModerateFDA (Drugs)·D-0635-2017·2017-04-12
Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) 90 mg extended-release tablets because residual sorafenib powder was found in the manufacturing equipment's inlet air duct.
Product
Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749601
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0626-2017·2017-04-12
GlaxoSmithKline Recalls Ventolin Inhalers Due to Defective Delivery System
GlaxoSmithKline is recalling 593,088 Ventolin inhalers because some units have out-of-specification leak rates, potentially affecting drug delivery.
Product
VENTOLIN — VENTOLIN (ALBUTEROL SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1747-2017·2017-04-12
Siemens ADVIA Centaur BR Assay Recalled for Potential Interference
Siemens Healthcare Diagnostics is recalling ADVIA Centaur BR assays due to potential interference from the Syphilis assay on the same systems.
Product
Siemens ADVIA Centaur BR assay Cat No. 02419937, SMN 10333349 (1-pack/50 tests) BR Assay for CA 27.29 The ADVIA Centaur¿ BR assay is an in vitro diagnostic test for the quantitative serial determination of cancer antigen CA 27.29 in human serum using the ADVIA Centaur¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1715-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Danish SRK. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1721-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi German SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2017·2017-04-12
Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling specific lots of Adalat CC (nifedipine) Extended-Release Tablets due to cross-contamination with sorafenib powder.
Product
Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 50419-70305
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1728-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Spanish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1708-2017·2017-04-12
Philips eCare Coordinator Software Recalled for Data Integrity Defects
Philips Visicu is recalling eCare Coordinator software due to a defect that may cause missing or redundant data to be saved without user notification.
Product
eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0631-2017·2017-04-12
Alvogen Recalls Nifedipine Tablets Due to Sorafenib Cross-Contamination
Alvogen Inc. is recalling Nifedipine Extended-Release Tablets, 90 mg, due to cross-contamination with sorafenib powder found in the inlet air duct.
Product
Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1706-2017·2017-04-12
Philips Recalls Mobile Diagnostic X-Ray Systems Due to Marker Placement Error
Philips Healthcare Inc. is recalling 220 Mobile Diagnostic X-Ray Systems because electronic markers may be placed at the wrong anatomical position when images are moved between views.
Product
Mobile Diagnostic X-Ray System with Digital Panel
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1719-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Errors
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi French SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1723-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Issues
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Japanese SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1733-2017·2017-04-12
Centurion Convenience Kits Recalled Due to Potential Sterile Packaging Breach
Centurion Medical Products is recalling Convenience Kits containing Curity Oval Eye Pads due to a potential breach in sterile packaging.
Product
EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
Category
Medical Device
Distribution
9 states
ModerateFDA (Devices)·Z-1717-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Dutch SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1716-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Czech SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1714-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi English SRK.. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1726-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Portuguese SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2017·2017-04-12
Adalat CC Tablets Recalled for Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets due to cross-contamination with sorafenib powder found in the manufacturing facility.
Product
Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0628-2017·2017-04-12
Adalat CC Tablets Recalled for Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets 30 mg due to cross-contamination with sorafenib powder.
Product
Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1724-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Italian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1722-2017·2017-04-12
Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits
Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.
Product
STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Greek SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0627-2017·2017-04-12
Alvogen Recalls Nifedipine Extended-Release Tablets Due to Sorafenib Cross-Contamination
Alvogen, Inc. is recalling Nifedipine Extended-Release Tablets, 30 mg, due to cross-contamination with sorafenib powder found in the manufacturing facility's inlet air duct.
Product
Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1753-2017·2017-04-12
Philips BrightView X Gamma Camera Recall Due to Brake Hub Assembly Error
Philips Medical Systems is recalling 27 BrightView X gamma cameras because a brake hub assembly error can cause the detector to backdrive.
Product
BrightView X 3/8 model number 882478 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
Category
Medical Device
Distribution
29 states