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. 2,889 recalls have been distributed to New York in the last 12 months.
Showing 1821–1840 of 30,153 recalls
Recalled Item: Centurion Sterile Weitlaner Retractor Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Four (4) total reports were sent to customers with clinically relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artix MT Thrombectomy Device Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487...
The Issue: Due to a software issue, the software may incorrectly process the date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US...
The Issue: Incorrect labeling in which the front red pouch label did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio 1 Granules for Filling ¿ 1 mm (2 cm¿) Recalled by SCIENCE & BIO...
The Issue: Vials of implant bone granules may contain less product then specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular software versions 6.x Recalled by Philips...
The Issue: An issue was identified with the software when using the Echo Module of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as...
The Issue: Disconnection of the adapter from the endotracheal tube can potentially be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...
The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atalante X Recalled by WANDERCRAFT SAS Due to Potential for exoskeleton to...
The Issue: Potential for exoskeleton to lose lateral balance and cause patient to fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.