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. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2646126480 of 30,153 recalls

Medical DeviceDecember 19, 2013· Biomet, Inc.

Recalled Item: Locking Cortical Screw 3.5mmX38mm Recalled by Biomet, Inc. Due to 3.5mmx38mm...

The Issue: 3.5mmx38mm Locking Cortical Screw, implants are being recalled since an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· ITC-Nexus Dx

Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...

The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Spacelabs Healthcare, Llc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Stryker Spine

Recalled Item: Specialty Straight Static Inserter Assembly Product Usage: This instrument...

The Issue: Stryker has received complaints from customers relating to fracture along...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control Recalled by...

The Issue: HORIBA Medical is informing all ABX PENTRA Urine Control L/H customers...

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

Class III — Low RiskOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: Possible break in the connector of the Force Sensor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems. Automated Recalled by...

The Issue: An overflow flag //// is displayed in the result column for a test when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 1.5MM x 7.5MM Cylindrical Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball Recalled by The...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 2MM Carbide Fluted Ball Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part #...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing