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. 2,386 recalls have been distributed to Hawaii in the last 12 months.
Showing 24501–24520 of 27,645 recalls
Recalled Item: Candela Laser GentleLase Pro Recalled by Candela Corporation Due to...
The Issue: Unintended single pulse maybe emitted to handpiece prior to pressing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Chemistry Systems models 1200 Recalled by Siemens Healthcare...
The Issue: The ADVIA Chemistry software systems using certain software versions allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems FOL Folic Acid Recalled by Siemens Healthcare...
The Issue: potential for an accelerated decline in counts per second (CPS) for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...
The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEAC Advanced Dental System Recalled by ASI Medical, Inc. Due to ASI Medical...
The Issue: ASI Medical is initiating a field correction for the SEAC Advanced Dental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC VORTX 2MM X 3MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucus Specimen Trap 40 cc Recalled by Medline Industries Inc Due to There is...
The Issue: There is a potential that the specified mucus specimen traps are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 90 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use...
The Issue: Stryker has identified a potential for the auger and/or cannula to fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin)...
The Issue: The patient label associated with the product may be incorrect in that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand SUPER COMPLIANT 4MM X 7MM Recalled by Stryker Neurovascular...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 150CM 2 TIP Recalled by Stryker Neurovascular...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.