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 28701–28720 of 52,535 recalls
Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: Broken or missing screws and retaining clips. This may be due to screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...
The Issue: Defective Container: Confirmed reports of loose vial crimps.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Packaging Services...
The Issue: Subpotent Drug: Out of specification for assay (stability testing)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....
The Issue: May contain endotoxin levels which have been confirmed to exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The device could have a missing spanner nut and snap ring which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...
The Issue: The device may process the same sample with two different sample IDs and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.