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. 2,689 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,689 in last 12 months

Showing 2026120280 of 55,896 recalls

FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***KOROMANTEE***Colonic & Intestinal Cleaner***used by the...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: Mitmitta (Cayenne Pepper) Recalled by Sundial Herbal Products Due to Recall...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***MANGO...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: SUNDIAL PRINCESS ALMAZ Traditional ETHIOPIAN Organic SPICED TEA Recalled by...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERB***SEA...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: "SUNDIAL***Jamaican & Tropical Raw Honey***" Recalled by Sundial Herbal...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: SUNDIAL ORGANIC JAMAICAN TUMERIC Recalled by Sundial Herbal Products Due to...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2020· Sundial Herbal Products

Recalled Item: ETHIOPIAN FLAX SEED OIL & HONEY BLEND Recalled by Sundial Herbal Products...

The Issue: Recall required by Order of Permanent Injunction. The products are...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 - Product Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris EtCO2 Module Model 8300 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris PCA Module Model 8120 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...

The Issue: Potential for sterile packaging to be compromised¿

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015. modular infusion pump and monitoring...

The Issue: If one or more screws or washers are loose or missing causing the battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Broken...

The Issue: Broken elements on pump module platen such as broken upper hinge post, lower...

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

Class I — Serious Health HazardOngoing