Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,099 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,099 in last 12 months

Showing 11621–11640 of 29,093 recalls

Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.24 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 8" (20 cm) Appx 0.53 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 135 cm (53") Ext Set w/Remv 5 Gang Stopcock 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: NanoClave Connector 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 2 Gang 4-Way NanoClave Stopcock Manifold w/Rotating Luer Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 9.5 IN (24cm)APPX 1.1ml SMALLBORE TRIFUSE SET 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 8 IN(20cm) APPX 0.46ml 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 3-Port NanoClave Manifold w/Check Valve 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 11 IN(28cm)APPX 0.7ml 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· Sysmex America, Inc.

Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...

The Issue: Insufficient amount of antibody without an error message or alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 128" (325 cm) Appx 16.6 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.32 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 112 IN(284cm) APPX 14.6ml 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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 11 IN(28cm)APPX 0.97ml 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.

Class II — Potential Health HazardOngoing