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. 2,580 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,580 in last 12 months

Showing 1800118020 of 52,000 recalls

Medical DeviceSeptember 11, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...

The Issue: There is a potential for the wrong patient information may be displayed in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2020· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: Failed Impurities/Degradation Specifications; high out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: ULTRA FAST-FIX AB ASSEMBLY - STRAIGHT-Absorbable Suture anchors Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· W L Gore & Associates, Inc.

Recalled Item: GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System...

The Issue: When the delivery catheter was attempted to be removed, there was an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: HEALICOIL RG SA 5.5MM W/2 UB-BL CBR BL-- Absorbable Suture Recalled by Smith...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA PLLA HA 6.5MM W/ NEEDLES- Absorbable Suture anchor Recalled by...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: BIORAPTOR 2.9MM SUTURE ANCHOR-Absorbable Suture anchor Product Number:...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA HA 6.5 W/2 UB (BLUE & BLK)- Absorbable Recalled by Smith &...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System *** EMPOWR Acetabular Cup Recalled by Encore...

The Issue: Due to incomplete machining a small peg remnant on the top of the dome that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BK-- Recalled by Smith & Nephew, Inc....

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX 6.5MM AB PRELOADED SUTURE ANCHOR- Absorbable Suture anchors Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX AB 5.0 SUTR ANCHR W/2 38 DURAB-Absorbable Suture anchors Recalled by...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA PLLA/HA 5.5 W/3 UB-Absorbable Suture anchor Product Number:...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX 6.5MM AB PRELOADED ULTRABRAID- Absorbable Suture anchors Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: RAPTORMITE 3.7MM AB W/ NEEDLES AND TWO-Absorbable Suture anchor Product...

The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...

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

Class II — Potential Health HazardOngoing