Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,895 recalls have been distributed to Rhode Island in the last 12 months.
Showing 6981–7000 of 27,456 recalls
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: 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: 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: MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter Recalled by...
The Issue: There is a potential leaking condition within the hub of affected devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...
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 Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...
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 Adult 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: 6.5 cm Adult 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: 6.5 cm Adult 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: Adult Craniotome Intended for cutting and shaping bone 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: 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: 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: 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: 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 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 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.
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 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 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: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...
The Issue: A software update (v1.1.5) has been developed to address the issue of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.