Hawaii Recalls

2,015 recalls on record affecting Hawaii

medical Class II
2026-05-27

C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc

Due to stain present on the surface of affected foley catheters.

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Food Class III
2026-05-13

Falcon Trading Co., Inc. recalls SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY

Potential contamination with pesticides, haloxyfop and thiamethoxam

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Food Class III
2026-05-13

Falcon Trading Co., Inc. recalls SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI

Potential contamination with pesticides, haloxyfop and thiamethoxam

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Food Class III
2026-05-13

Falcon Trading Co., Inc. recalls SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY

Potential contamination with pesticides, haloxyfop and thiamethoxam

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medical Class II
2026-05-06

Straumann USA LLC recalls Straumann n!ce PMMA Full-arch Restoration. Screw-retained Br

Includes an incorrect screw seat interface.

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medical Class II
2026-05-06

Straumann USA LLC recalls Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.01

Includes an incorrect screw seat interface.

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Food Class I
2026-04-29

Unistel Industries Inc. recalls SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel In

Product may be contaminated with Salmonella.

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medical Class II
2026-04-15

Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quic

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

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medical Class II
2026-03-18

Exactech, Inc. recalls Brand Name: Equinoxe Product Name: Equinoxe Core Instrumen

Impactor handle may be missing cross-pin

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medical Class II
2026-03-18

Exactech, Inc. recalls Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impact

Impactor handle may be missing cross-pin

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medical Class II
2026-04-08

Ultradent Products, Inc. recalls Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 70

Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.

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Food Class III
2026-03-25

Winder Laboratories, LLC recalls Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx

Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.

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Food Class II
2026-04-08

Imu-Tek Animal Health, Incorporated recalls Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally

Product is potentially under-processed.

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Food Class II
2026-04-08

Imu-Tek Animal Health, Incorporated recalls Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day

Product is potentially under-processed.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls The OEC 9900 Elite mobile fluoroscopy system is designed to

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 680

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-18

GE OEC Medical Systems, Inc recalls OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is des

GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.

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medical Class II
2017-01-25

DICOM GRID INC recalls Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R S

A software error caused the window/level to become the same in one series regardless if the image had different levels; image results have a washed-out grey appearance.

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medical Class II
2017-01-25

The Binding Site Group, Ltd. recalls Human Lambda Free SPAPlus Kit Product Code: LK018.S Fr

Calibration curve activity has increased over time in the kit lots listed.

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medical Class II
2017-02-01

INO Therapeutics (dba Ikaria) recalls Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery syste

Mallinckrodt discovered that some devices may have been manufactured with an out-of-tolerance manometer which can result in in an inaccurate proportional valve calibration table in an affected device.

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Showing 20 of 2,015 recalls. Use search to filter further.