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. 2,674 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,674 in last 12 months

Showing 2898129000 of 52,535 recalls

Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...

The Issue: if the cables of the Monica IF24 System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2017· Kalila Medical

Recalled Item: Vado Bi-Directional Steerable Sheath 8.8F Recalled by Kalila Medical Due to...

The Issue: Torn sheath liner material was detected at the proximal end of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2017· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008 K2 Hemodialysis Machine with software version 5.40 Recalled by...

The Issue: When the recirculation ultrafiltration (UF) Goal is set to a value greater...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2017· Kalila Medical

Recalled Item: Vado Steerable Sheath 8.8F Recalled by Kalila Medical Due to Torn sheath...

The Issue: Torn sheath liner material was detected at the proximal end of the device...

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

Class II — Potential Health HazardOngoing
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Teva Pharmaceuticals USA

Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications: High out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 13, 2017· ALLERGAN

Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...

The Issue: Failed Stability Specifications: Product stability testing results did not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 13, 2017· Covidien LLC

Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...

The Issue: Product reportedly shutting down during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2017· Halyard Health, Inc

Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...

The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...

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

Class II — Potential Health HazardOngoing
FoodDecember 13, 2017· Harrisburg Dairies, Inc

Recalled Item: 365 brand Egg Nog Recalled by Harrisburg Dairies, Inc Due to Dried Egg Yolks...

The Issue: Dried Egg Yolks was not specifically stated in ingredient statement

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED Whitefish Meat Recalled by Rachael's Food Corporation Due...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Traditional Kippered Salmon Recalled by Rachael's Food Corporation Due to...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Smoked Salmon packed under Springfield Smoked Fish and Rachael's: - Recalled...

The Issue: Product tested positive for Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Rachael's SPRINGFIELD SMOKED FISH Smoked Trout 6 oz Recalled by Rachael's...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund