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. 2,590 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,590 in last 12 months

Showing 4262142640 of 52,535 recalls

Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...

The Issue: Device may malfunction, which could cause therapy to be delayed, disabled,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· KCI USA, INC.

Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...

The Issue: KCI has received reports that, in a small number of cases, the CelluTome...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Horiba Instruments Inc

Recalled Item: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and...

The Issue: HORIBA Medical is informing all HORIBA Medical Lite DM customers using...

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

Class II — Potential Health HazardOngoing
FoodNovember 18, 2014· Tastefully Simple, Inc

Recalled Item: Product comes in as part of Fabulous Fudge Gift Box. Recalled by Tastefully...

The Issue: Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 17, 2014· Nutri-Dyn Midwest, Inc.

Recalled Item: Nutri-Dyn Recalled by Nutri-Dyn Midwest, Inc. Due to Mislabeling

The Issue: Nutri-Dyn has initiated a recall due to mislabeling. During production of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 17, 2014· Karlsburger Foods, Inc.

Recalled Item: Karlsburger Foods Low Sodium Taco Seasoning Recalled by Karlsburger Foods,...

The Issue: Taco Seasoning has an allergen of milk in the product that is not declared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2014· Karlsburger Foods, Inc.

Recalled Item: Karlsburger Foods Taco Seasoning Recalled by Karlsburger Foods, Inc. Due to...

The Issue: Taco Seasoning has an allergen of milk in the product that is not declared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Halyard Health

Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...

The Issue: The cuff inflation line may detach from the endotracheal tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2014· Stryker Endoscopy

Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...

The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...

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

Class II — Potential Health HazardOngoing