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. 1,037 recalls have been distributed to Maryland in the last 12 months.
Showing 25001–25020 of 52,535 recalls
Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angled Tip Ureteral Catheter Set Recalled by Cook Inc. Due to The wire guide...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Recalled by Ardent Mills, LLC Due...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARDENT H&R SR FLR Recalled by Ardent Mills, LLC Due to Potential Salmonella...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Recalled by Ardent Mills, LLC...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: King LTS-D Kit Size 1 Recalled by King Systems Corp. dba Ambu, Inc. Due to...
The Issue: Size 0 products were incorrectly packaged and labeled as a size 1 products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...
The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...
The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.