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. 1,834 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,834 in last 12 months

Showing 4214142160 of 55,896 recalls

FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Coastal Harbor Oak & Beechwood Smoked Salmon Sliced Side Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Wild River Pacific Smoked Salmon 4oz. D-Cut Products are Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Cambridge House Mild Smoked Salmon Sliced Side - Grade Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: Cambridge House Royal Smoked Salmon Sliced Side Products are packaged...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Private Reserve Rope Hung Smoked Scottish Salmon 4oz. Products Recalled by...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Baxter Healthcare Corp

Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug; out of specification results for heparin raw material

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: WIZARD2 5-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Omnilife Science Inc.

Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...

The Issue: Product may breach the inner and outer sterile pouches during shipping or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Biomet, Inc.

Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...

The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Stryker Endoscopy

Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...

The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing