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. 2,648 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,648 in last 12 months

Showing 3098131000 of 55,896 recalls

Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· GE Medical Systems China Co., Ltd.

Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...

The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...

The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Crimson Trace Corporation

Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...

The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Karl Storz Endoscopy

Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...

The Issue: The label outside the cardboard box is labeled correctly but the pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...

The Issue: One reported complaint and discovered that the outer vial was out of round...

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

Class II — Potential Health HazardOngoing
FoodOctober 10, 2017· La Terra Fina, Inc.

Recalled Item: La Terra Fina Spinach Artichoke & Parmesan Dip & Spread Recalled by La Terra...

The Issue: Undeclared allergen; egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: VANCOmycin 1.5 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Ropivacaine HCL (PF) 0.2% (2mg/mL) 100 mL Cassette Rx Only Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Midazolam HCL 100 mg (1mg/mL) 100 mL Cassette in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentanyl citrate (PF) 1100 mcg (20 mcg/mL) 55 mL syringes Recalled by Banner...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Succinylcholine 200 mg/10 mL Syringe Recalled by Banner Pharmacy Services,...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: OXYtocin 30 units added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund