Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,077 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,077 in last 12 months

Showing 11001–11020 of 47,764 recalls

Medical DeviceJuly 26, 2022· Abbott Laboratories

Recalled Item: ARCHITECT STAT Troponin-I Reagent Kit Recalled by Abbott Laboratories Due to...

The Issue: One lot of reagent was manufactured with insufficient quantities of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Isopure Corp

Recalled Item: Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified...

The Issue: Acidified Concentrate Distribution System potential electrical safety hazard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Medtronic Neuromodulation

Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...

The Issue: Potential communication issue in which the Vanta Clinician Programmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2022· Medtronic Neuromodulation

Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...

The Issue: Potential for Vanta Clinician Programmer Application (CP App) A71200...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5" Recalled by Stradis...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Nobel Biocare

Recalled Item: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm Recalled by Nobel Biocare Due to...

The Issue: Due to the presence of a burr which may cause an aspiration risk to patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" Recalled by Stradis Medical,...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...

The Issue: The sterile barrier may be compromised.

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2022· SterRx, LLC

Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride Recalled by SterRx, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2022· SterRx, LLC

Recalled Item: FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Delayed-Release Oral Suspension*40 mg* suspension in...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2022· Distributor RFR, LLC.

Recalled Item: SANGTER Energy Supplement Capsules Recalled by Distributor RFR, LLC. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Corin Ltd

Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...

The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing