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. 2,221 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,221 in last 12 months

Showing 32613280 of 55,896 recalls

Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· B Braun Medical Inc

Recalled Item: Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in. Recalled by B Braun...

The Issue: Increased risk for valve housing detachment causing leakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Simethicone 20 mg per 0.3 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Morphine Sulfate 5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 17, 2025· Kenover Marketing Corp.

Recalled Item: Glicks Dark Chocolate Conettos Recalled by Kenover Marketing Corp. Due to...

The Issue: Undeclared Allergen (Milk)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 36 Coated Super Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month Heavy Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Super and 18 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Regular and 9 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing