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. 999 recalls have been distributed to New York in the last 12 months.
Showing 45741–45760 of 55,896 recalls
Recalled Item: Hydrocortisone base active pharmaceutical ingredient packaged in varying...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED) Recalled by The Anspach Effort, Inc. Due...
The Issue: May operate solely in reverse mode, not operate in reverse mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLUTTER Percussor respiratory device Recalled by Aptalis Pharmatech Inc. Due...
The Issue: Customer notification that the device may be difficult to open or close.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml...
The Issue: Use of the product could result in inadequate recovery of Legionella...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Reagent Container Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: HORIBA Medical is recalling the ABX PENTRA 400 Reagent Container because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Revolution CT is a multi-slice (256 detector row) CT Recalled by GE...
The Issue: A required quality control test was not performed during installation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView model number: 882478 BrightView X model number: 882480 BrightView...
The Issue: Unintended detector and gantry movement due to software issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. The IM...
The Issue: Use of excessive force when impacting may lead to intra-operative femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beachbody Hardcore Base Shake Lot #42932B22 Recalled by Beachbody Llc Due to...
The Issue: During an investigation of label issuance and reconciliation at the firm's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GENTAMICIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Defective...
The Issue: Defective Container: Vials may be missing stoppers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...
The Issue: The product is sold and labeled as EO sterilized, however the units were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...
The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...
The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlignRT is a video-based three-dimensional (3D) surface imaging system which...
The Issue: Potential use error when the external Gate Controller is turned ON after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...
The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.