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.
Showing 28041–28060 of 29,093 recalls
Recalled Item: Fitmore" Hip Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kopf Adapter S Sterile Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿ cancellous screw Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Original M.E. Mueller" Low Profile Cup Sterile Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30¿ Distal centralizer Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Humeral stem Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30¿ Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ Revision + set screw Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Inverse/Reverse Glenoid Sterile Recalled by Zimmer,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Inverse Humeral Cup Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: zimmer Anatomical Shoulder Glenoid S Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox¿ Option Ceramic Femoral Head System Rx Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile Recalled by...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alloclassic SL Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump Recalled...
The Issue: Accuro has received reports of some Apex Pumps either failing to operate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup Liner 22 mm LD. Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc. is initiating a removal of the Multipolar¿ Bipolar Cup Liner 22...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT Big Bore is a whole-body Computed Tomography Recalled by...
The Issue: Philips Healthcare received a complaint stating the system opens e-stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.