Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,923 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,923 in last 12 months

Showing 2562125640 of 29,208 recalls

Medical DeviceDecember 19, 2013· Teleflex Medical

Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.

The Issue: Sterility cannot be guaranteed.

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 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· 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· 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· 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· 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· 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· 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· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine...

The Issue: Bicarbonate Jug Adapter distributed prior to 510(k) approval

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: 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: 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: 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: 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
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 50 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100S Sterilization System Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue which...

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

Class II — Potential Health HazardOngoing