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. 2,517 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,517 in last 12 months

Showing 1024110260 of 27,456 recalls

Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 6MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: KD-612U ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 6MMx 23G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: KD-612L ELECTROSURGICAL KNIFE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 6MMx 25G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: B7-2C BALLOON CATHETER 13mm dia 2.8 Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 26G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-400U-10 SNAREMASTER PLUS Hot/Cold 10m Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 6MMx 21G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 1.8MMx 26G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 5MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 6MMx 25G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 4MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2MM CH 23G 6MM Recalled by Aomori Olympus Co., Ltd. Due...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: B-V243Q-A 3-LUMEN EXTRACTION BALLOON V Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: CRESCENT SNARE Recalled by Aomori Olympus Co., Ltd. Due to Inspection...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-411D-1521 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing