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. 2,619 recalls have been distributed to Maryland in the last 12 months.
Showing 38841–38860 of 52,535 recalls
Recalled Item: Shorts on The Beach Strong Formula by Pink Bikini capsules Recalled by...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Bikini Strong Formula capsules Recalled by Lucy's Weight Loss (dba....
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Element Press-Fit Recalled by Exactech, Inc. Due to Eight (8)...
The Issue: Eight (8) pieces did not receive the specified Hydroxyapatite (HA) coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets...
The Issue: Cross Contamination With Other Products: Potential cross-contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TASTEE Plain Caramel Apple Recalled by Tastee Apple Inc Due to The firm was...
The Issue: The firm was notified by a customer that their Plain Caramel Apples contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge Cardio software with Issuer of Patient ID (IPID). The Recalled by...
The Issue: For sites using the Issuer of Patient ID (IPID), the system will display the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: Users can merge a device import file with an image study that already has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 100 system included the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 300 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sentinel MULTIGENT Ammonia Ultra Reagent Recalled by Sentinel CH SpA Due to...
The Issue: Results for ammonia are below the linear range of the assay for samples that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Bone Marrow Biopsy Trays Catalogue No. 3404253 Various medical...
The Issue: Integra received an Urgent Drug Recall Notice from Hospira Inc. for their 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Omega 3 Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Vitamin D Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is...
The Issue: One mislabeled dose of TheraSphere¿ Y-90 Glass Microspheres, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valeant Pharmaceuticals North America Recalled by Valeant Pharmacueticals...
The Issue: The Serial I.D. Label and some information in the Operation Manual for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.