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. 2,648 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,648 in last 12 months

Showing 3486134880 of 52,535 recalls

Medical DeviceAugust 10, 2016· Medline Industries Inc

Recalled Item: Rigid Suction Canister 3000 CC and 2000 CC. Recalled by Medline Industries...

The Issue: Risk of implosion when the Rigid Suction Canister is subjected to excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: 5 Port OFF Manifold with Transpac IV Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: SafeSet Kit with 30 mL Flush Device Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Pediatric Kit with 30mL Flush Device Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Kit With Safeset Reservoir And 2 Blood Sampling...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit with 03mL Flush Device Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with SafeSet Reservoir and Blood Sampling Port...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Blood Sampling Ports Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Monitoring Kit with 2 SafeSet Reservoir and 2 Blood Sampling...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc. Due to...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Single Monitoring Kit with 30mL Flush Device Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: Transpac IV Trifurcated Monitoring Kit with SafeSet Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2016· ICU Medical, Inc.

Recalled Item: TP4 Kit with 10cc SafeSet Reservoir Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2016· Allergy Laboratories, Inc.

Recalled Item: Ephedrine Sulfate Injection Recalled by Allergy Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility: An FDA inspection at the facility raised...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: Communication provided to emphasize that the PSA values should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...

The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders...

The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Mentor Texas, LP.

Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...

The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2016· Zimmer Biomet, Inc.

Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...

The Issue: Contents of the package do not match the product labeling. Product is...

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

Class II — Potential Health HazardOngoing