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.
Showing 7001–7020 of 27,645 recalls
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS IR...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: a) MEDLINE HAND PACK Recalled by...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE PLASTICS/PEDS KIT Recalled by...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: a) MEDLINE PERF. ASSOC. CUT DOWN TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with Recalled...
The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...
The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball bearings...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Shoulder System Resection Planer 35mm Resection Planer Recalled by...
The Issue: Two planers were found to be unusable during sawbones shoulder training.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobiCT-32 AIRO Mobile CT Scanner Recalled by Mobius Imaging, LLC Due to...
The Issue: Stryker received one report of an injury to an untrained user that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.