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. 2,702 recalls have been distributed to Maryland in the last 12 months.
Showing 22781–22800 of 29,093 recalls
Recalled Item: HDL-Cholesterol plus gen.3. Recalled by Roche Diagnostics Operations, Inc....
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus ver. 2. Intended for use on COBAS INTEGRA systems Recalled...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides/Glycerol Blanked. In vitro test for the quantitative...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (enGen System) Recalled by Ortho-Clinical...
The Issue: Recapper Caps may fall off of, or be knocked from sample tubes placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 Diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Signal Reagent Recalled by ORTHO-CLINICAL...
The Issue: The Immunodiagnostic Products Signal Reagent, Lot 3082 as the reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...
The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.