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. 2,584 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,584 in last 12 months

Showing 4420144220 of 52,535 recalls

Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2014· Bracco Diagnostic Inc

Recalled Item: E-Z-HD (barium sulfate) For Suspension (98% w/w) Recalled by Bracco...

The Issue: Subpotent Drug: Low out of specification results for both pH and assay...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Mentor Texas, LP.

Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...

The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Smith & Nephew, Inc.

Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....

The Issue: There was an error in manufacturing which resulted in the proximal lag screw...

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

Class II — Potential Health HazardOngoing
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Ibuprofen Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Oxcarbazepine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: HyVee applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile S.A....

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Cinnamon Recalled by PUREFRUIT CHILE S.A Due to...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2014· Biomet, Inc.

Recalled Item: Vanguard 360 Femoral Boss Reamer Recalled by Biomet, Inc. Due to The...

The Issue: The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Ansar Group, Inc. Dba Ansar Medical Technologies, Inc

Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...

The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Zimmer, Inc.

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...

The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· PerkinElmer Health Sciences, Inc.

Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...

The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9

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

Class II — Potential Health HazardOngoing