Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,868 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,868 in last 12 months

Showing 45614580 of 30,153 recalls

Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device:...

The Issue: Degraded and unusable upon removal from the foil pouch due to exposed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Innomed, Inc.

Recalled Item: INNOMED CUP REMOVAL STARTER INSTRUMENT Recalled by Innomed, Inc. Due to 54...

The Issue: 54 MM finisher blade was inadvertently affixed to the shaft of the CupX...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Humeral Liner: Item Numbers: a) 320-40-00 Recalled by...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Outset Medical, Inc.

Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...

The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing