Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,098 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
1,098 in last 12 months

Showing 19501–19520 of 55,896 recalls

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

Recalled Item: OSTEORAPTOR 2.9 W/ 1 UB COBRAID 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: OSTEORAPTOR 2.3 W 1UB II 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: 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
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· 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: 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· 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
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Buttered microwave popcorn packaged in the following ways: 1) Full Recalled...

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Lightly salted microwave popcorn packaged in the following ways: 1) Recalled...

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Light microwave popcorn packaged in the following ways: 1) Full Recalled by...

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Microwave popcorn packaged in the following ways: 1) Full Circle Recalled by...

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Cadia Organic Unsalted Microwave Popcorn Recalled by Gilster-Mary Lee Corp....

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2020· Lidl US TRADING

Recalled Item: Lidl Organic Butter Microwave Popcorn Recalled by Lidl US TRADING Due to...

The Issue: Lidl US, LLC has initiated a recall of Lidl Organic Butter Microwave...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund