Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,659 in last 12 months

Showing 1106111080 of 28,334 recalls

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

Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- 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: 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· 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· 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: 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 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: ULTRA FAST-FIX AB ASSEMBLY-REVERSE CURVE-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 5.5 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 ULTRA PLLA HA 4.5MM 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: 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: 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: 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: 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 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 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: 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· 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: 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· 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 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