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 28861–28880 of 29,093 recalls
Recalled Item: GE Recalled by GE Healthcare, LLC Due to Fastener bolts on the heat...
The Issue: Fastener bolts on the heat exchanger were not properly torqued and part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL3 SOFT-TISSUE Laser (Model LR2002) Recalled by Discus Dental LLC Due to...
The Issue: The firm is initiating this recall of the SL3 Soft Tissue Laser equipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of an issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medpro Elastomeric Infusion Pump. AccuFlux Recalled by First Medical Source...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model...
The Issue: Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set stability claim...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sigma Spectrum VOLUMETRIC INFUSION PUMP Recalled by Baxter Healthcare...
The Issue: Recall expansion; the infusion pumps have the potential to fail causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 4.0mm Contour ,1mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: Recalled by...
The Issue: Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Irrigation Set labeled in part: ***24K Arthroscopy Outflow/Suction...
The Issue: ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc Blood Analysis BGEM Test Cards for use with the Recalled by Epocal Inc...
The Issue: Customer reported problem while performing incoming QC of newly received lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console***SN G 10307653002*** Product Usage: The Recalled...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Volumetric Infusion System. For intravenous infusion of parenteral...
The Issue: Update Instruction For Use for Preventative Maintenance (PM) Schedule and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian High Energy Clinacs Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: Under certain conditions, photon beams in High Energy Clinacs may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component (Smith...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Recalled...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.