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. 2,496 recalls have been distributed to Rhode Island in the last 12 months.
Showing 11181–11200 of 27,456 recalls
Recalled Item: Mako Hip End Effector Recalled by Mako Surgical Corporation Due to...
The Issue: Characterization issue associated with the product. This issue may cause a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...
The Issue: Potential risk of brush detachment during cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...
The Issue: The plastic housing on the device may fracture
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 IN (33cm) APPX 0.96 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 IN(33cm) APPX 1.0 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx 0.35 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.