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. 2,716 recalls have been distributed to Maryland in the last 12 months.
Showing 22101–22120 of 29,093 recalls
Recalled Item: Model 5001102 MPS Delivery Set w/ arrest agent and additive cassettes...
The Issue: The products have been found to intermittently exhibit a seal failure during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DGDE Recalled by Implant Direct Sybron Manufacturing, LLC Due to Implant...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling 26 lots of DGDE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential issue with routine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon Dry Acid Dissolution Unit Recalled by Fresenius Medical...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iOS Galileo Application Version 1.1.1 or lower that programs the Recalled by...
The Issue: A software issue can make the foot move into dorsiflexion, unnoticed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...
The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The...
The Issue: Incorrect use of T-Piece resuscitators will result in complete occlusion of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans Recalled...
The Issue: Monitor may shut down unintentionally without restarting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 7F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.