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. 1,067 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,067 in last 12 months

Showing 29681–29700 of 55,896 recalls

DrugMarch 15, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Failed Dissolution Specifications; during stability testing

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2018· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...

The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 15, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...

The Issue: Failed Dissolution Specifications; during stability testing

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2018· Biocare Medical, LLC

Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...

The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...

The Issue: An issue with one of the electric components (a resistor) could result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Polymer Technology Systems, Inc.

Recalled Item: PTS Panels¿ CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...

The Issue: Potential for loss of activity of the glucose analyte (under-recovery) prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Invivo Corporation

Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...

The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...

The Issue: The cap on the vial might be labeled with the incorrect part number but the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...

The Issue: There is an increased risk of false positive Proteus results when the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corp.

Recalled Item: Philips HeartStart FRx AED. Recalled by Philips Electronics North America...

The Issue: An issue with one of the electric components (a resistor) could result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...

The Issue: After continuous operation for more than one and a half days, the image on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...

The Issue: The firm received complaints of drill bits breaking during use with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMarch 13, 2018· Mondelez Global Llc

Recalled Item: Sour Patch Kids Recalled by Mondelez Global Llc Due to Mondelez Global LLC...

The Issue: Mondelez Global LLC is initiating a recall because remnants of a half peanut...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 12, 2018· Food and Beverage Inc.

Recalled Item: Name: Trader Joe s Chocolate Chip Cookies SKU 68075 Net Recalled by Food and...

The Issue: Food & Beverage Inc., dba Chris's Cookies has initiated a recall of Trader...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· McKesson Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by McKesson Israel Ltd. Due to Change...

The Issue: Change Healthcare has identified an issue where, under certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing