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 28641–28660 of 52,535 recalls
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile EXACTAMED Oral Dispenser Recalled by Baxter Healthcare Corporation...
The Issue: Affected lot of 5 mL oral dispensers was packaged in individual pouches that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYMUTEST HIA MonoStria qualitative screening assay intended for the global...
The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYMUTEST HIA IgGAM Recalled by Hyphen BioMed Due to Incorrect package insert...
The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYMUTEST HIA MonoStrip IgG Recalled by Hyphen BioMed Due to Incorrect...
The Issue: Incorrect package insert indicating use of the kits with plasma, serum, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...
The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Recalled by eBars...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GOLF ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ Recalled by eBars Due...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT. 1.6 OZ (45g) Recalled by eBars...
The Issue: The product test positive for peanut allergen which is not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 Recalled by...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.