Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2852128540 of 29,188 recalls

Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2012· Synthes (USA) Products LLC

Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...

The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· SALTER LABS

Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...

The Issue: A complaint was received, and later verified, that product labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· Abbott Laboratories

Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...

The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Microbiologics Inc

Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...

The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· GE Healthcare, LLC

Recalled Item: Advantage Workstation Volume Share 2 (versionAW4.4_04) with Volume Viewer 3...

The Issue: GE Healthcare has became aware of two issues with the Advantage Workstation....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Alphatec Spine, Inc.

Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...

The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Alcon Research, LTD.

Recalled Item: This voluntary medical device correction is related to Alcon products...

The Issue: This medical device correction is related to Alcon products that present a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...

The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...

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

Class III — Low RiskOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...

The Issue: When using the syngo Quality Control package the system may not perform as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....

The Issue: When using the EasyLink Quality Control Package the system may not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Mckesson Medical Imaging Group

Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...

The Issue: There is a potential to save reports in RadReport with an Incorrect Final...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· IDEV Technologies, Inc.

Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...

The Issue: There was an error on the outer labeling of this device. The inner label was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2012· CareFusion 303, Inc.

Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...

The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume...

The Issue: Incorrect views and measurements possible. GE Healthcare became aware of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...

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

Class II — Potential Health HazardOngoing