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. 2,637 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,637 in last 12 months

Showing 1458114600 of 29,188 recalls

Medical DeviceMarch 20, 2019· GETINGE US SALES LLC

Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...

The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes

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

Class III — Low RiskOngoing
Medical DeviceMarch 19, 2019· GE Healthcare, LLC

Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...

The Issue: The outer seam of the coil, closest to the system cable, may separate and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Collagen Matrix, Inc.

Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...

The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Carestream Health, Inc.

Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...

The Issue: When the user performs the re-assignment of a parent / companion pair, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...

The Issue: During manufacture, packaging materials for a small portion of the lot may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Ideal Implant Incorporated

Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...

The Issue: The implants were deflating due to a piece of silicone disrupting the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...

The Issue: Continuous operation at very high tube output may result in increased wear...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Roche Diagnostics Corporation

Recalled Item: Albumin BCP Product Usage: ALBP is an in vitro test Recalled by Roche...

The Issue: The reagent lot is exhibiting calibration failures, QC imprecision, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· Response Biomedical Corp.

Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...

The Issue: The form received three complaints related to the user obtaining a result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· Roche Diagnostics Corporation

Recalled Item: cobas e 801 immunoassay analyzer Recalled by Roche Diagnostics Corporation...

The Issue: The firm has confirmed complaints regarding signal drops on the cobas e 801...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· Cytocell Ltd.

Recalled Item: Aquarius CSF1R/RPS14 (5q32-q33) Probe Red Recalled by Cytocell Ltd. Due to...

The Issue: There is an error in the chromomap included in the labeling for the product.

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

Class III — Low RiskOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 6 Recalled by GE Healthcare, LLC Due to There is a potential for...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing