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. 2,619 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,619 in last 12 months

Showing 3700137020 of 55,896 recalls

Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 28CM Item Code: E278128 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode Retractable 28CM Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Argon Sharp Needle Electrode 28CM Item Code: E258228...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Straight Spatula Electrode 36C Item Code: E277036 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 6" Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Argon Modified Flat l Electrode 28CM Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· BioMerieux SA

Recalled Item: NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products...

The Issue: Several customer complaints about amplification performance issues when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Straight Spatula Electrode 28CM Item Code: E278028...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Cylindrical Tip Electrode 28CM Item Code: E278628 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode 36CM Item Code: E277436 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...

The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· T2 Biosystems Inc

Recalled Item: T2Candida¿Cartridges Recalled by T2 Biosystems Inc Due to Elevated levels of...

The Issue: Elevated levels of invalid results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Arrow International Inc

Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...

The Issue: Arrow is recalling due to incorrect labeling of products.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...

The Issue: This field action is being initiated following the firm's discovery of a...

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

Class III — Low RiskOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· TZ Medical, Inc.

Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...

The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2016· Safecor Health, LLC

Recalled Item: Doxycycline100mg Tablets Recalled by Safecor Health, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 7, 2016· Safecor Health, LLC

Recalled Item: Acetaminophen 325mg tablets Recalled by Safecor Health, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund