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. 900 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
900 in last 12 months

Showing 53101–53120 of 55,896 recalls

Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 12 x 40 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...

The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left)...

The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...

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

Class II — Potential Health HazardOngoing
FoodJanuary 11, 2013· Jiffy Food Service, LLC

Recalled Item: Spice Cake Mix Recalled by Jiffy Food Service, LLC Due to Undeclared Allergen

The Issue: Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 11, 2013· AstraZeneca LP

Recalled Item: PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30...

The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 11, 2013· AstraZeneca LP

Recalled Item: PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation...

The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2013· Hospira, Inc.

Recalled Item: Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2013· GE Healthcare, LLC

Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of an incident which caused a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2013· Allergen Medical

Recalled Item: SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN. Surgical mesh...

The Issue: Product is dual packaged in an inner and outer pouch, the outer pouch seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2013· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...

The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...

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

Class I — Serious Health HazardOngoing
DrugJanuary 8, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights ALMOND Natural Flavor Coconut Haystacks Recalled by Island...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks Recalled by...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 8, 2013· Island Delights, Inc.

Recalled Item: Island Delights Almond Chocolate/Almond Mix Natural Flavor Coconut Haystacks...

The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 7, 2013· Somersault Snack Co., LLC

Recalled Item: Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds...

The Issue: During ingredient review for kosher certification, the firm discovered that...

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

Class I — Serious Health HazardOngoing
Refund