Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,703 recalls have been distributed to New York in the last 12 months.
Showing 21001–21020 of 30,153 recalls
Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...
The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# 4001-00 The Anastoclip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one...
The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2 over 2 Elevating Monitor Suspension - Omega Medical Imaging Recalled by...
The Issue: Elevating Monitor Suspension separated from the lifting column bracket
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed...
The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom REG implants Sterile The Axiom REG implants are used Recalled by...
The Issue: Following a FDA inspection showing that the firm failed to validate the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...
The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom 2.8 implants Sterile The Axiom REG implants are used Recalled by...
The Issue: Following a FDA inspection showing that the firm failed to validate the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that that the selected Plan-of-the Day could be accidently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.