Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,609 in last 12 months

Showing 1110111120 of 28,748 recalls

Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR-Absorbable Suture anchors 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 5.0MM AB SUTURE ANCHOR WITH TWO- Absorbable Suture anchors Recalled...

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: OSTEORAPTOR 2.3 W. UB COBRAID BLUE-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: HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BL-- 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: OSTEORAPTOR 2.3 W/ 1 UB COBRAID BLACK-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
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: TWINFIX ULTRA HA 4.5 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· Smith & Nephew, Inc.

Recalled Item: TWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO Absorbable Suture anchors Recalled...

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
Medical DeviceSeptember 9, 2020· Smith & Nephew, Inc.

Recalled Item: OSTEORAPTOR 2.9 W. 2 UB WHITE / BLACK -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: MICRORAPTOR REGENESORB SUTURE ANCHOR- 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
Medical DeviceSeptember 9, 2020· W L Gore & Associates, Inc.

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

The Issue: Due to secondary deployment fiber being attached to secondary deployment...

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 5.5MM W/1 UT & 1 UB BL- 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: HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BL- 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 ULTRA 6.5MM PLLA/HA 2 UBWHT/BL-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
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: ULTRA FAST-FIX AB ASSEMBLY - CURVED-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: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- 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: TWINFIX ULTRA PLLA/HA 6.5 W/3 UB- Absorbable Suture anchor Product Recalled...

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 ULTRA-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: HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- 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