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. 2,100 recalls have been distributed to New York in the last 12 months.
Showing 6981–7000 of 30,153 recalls
Recalled Item: Titan Touch Scro Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shanghai United Imaging Healthcare Co. Recalled by Shanghai United Imaging...
The Issue: Due to a software issue where the process of patient scanning, the scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...
The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...
The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Re-optimization, after adding contours without forced density outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...
The Issue: The external diameter of the biopsy instrument is larger than the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RelieVR Recalled by Appliedvr Due to There is the potential for the program...
The Issue: There is the potential for the program software to malfunction which will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...
The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...
The Issue: Problem maintaining the stable placement of the battery may come loose from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iradimed Corporation MRidium MRI 1000 Series Infusion Sets Recalled by...
The Issue: Certain Iradimed 1057 Syringe Adapter Sets, used with the MRidium MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor is a portable vital signs monitor Recalled by...
The Issue: During internal testing, Regulatory Compliance issues were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable...
The Issue: There have been complaints that the clip did not come out of the tube sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and Recalled by...
The Issue: Mislabeled: Product is marked with GTIN # 04046955299592 however; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Peritoneal Dialysis System. Used for automatic control of dialysis...
The Issue: The electrical safety testing was not properly performed on the impacted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...
The Issue: Engaging titanium base contains a dimensional condition that allows vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.