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. 1,084 recalls have been distributed to Maryland in the last 12 months.
Showing 15041–15060 of 52,535 recalls
Recalled Item: QIAcube Connect MDx Recalled by Qiagen Sciences LLC Due to During the "Load...
The Issue: During the "Load tip racks and enzymes" step of the run set-up, the info...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ripple Dairy-Free. As It Should Be 8g Plant Based Protein Recalled by RIPPLE...
The Issue: Complaint led investigation found the presence of Bacillus Cereus in one lot...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Birds Eye Broccoli Tots Recalled by CONAGRA BRANDS Due to Small rocks and...
The Issue: Small rocks and metal fragments in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...
The Issue: There have been reports of stent migration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD series with Software Version Number: 2.1.x- Recalled...
The Issue: Set screws securing the two gliding rods of the Extra Monitors (called 7th...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Direct Amplification Disc Kit Recalled by DiaSorin Molecular LLC...
The Issue: A subset of affected discs are at risk of leakage when it is used more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS-Computed tomography system Model 8098027 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence -Computed tomography systems Model 10590100 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Subpotent...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA...
The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...
The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to Recalled...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core LASIK Pack 2-Medical Kit- intended to be Recalled by Beaver...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core SMILE Pack 1-Medical Kit intended to be Recalled by Beaver...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNANAIL MINI Recalled by Medshape, INC. Due to The firm identified a...
The Issue: The firm identified a nonconformance in Lot 04882 involving the endcap being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Kit intended Recalled by...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core Phaco Pack 1-Medical Cataract Kit intended to be Recalled by...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.