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. 2,787 recalls have been distributed to Maryland in the last 12 months.
Showing 16941–16960 of 29,093 recalls
Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...
The Issue: Failure to follow proper charging practices can result in lithium-ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...
The Issue: This recall has been identified due to the batch being mislabeled, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to Recalled by Dako...
The Issue: To correct the kit's instructions for use as the storage time for gastric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope ( Model 10967666) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 (Model 10165888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective 16 (Model 10891666) Recalled by Siemens Medical...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Power (Model 10967888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 (10165977) Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...
The Issue: Packaged with an incorrect overwrap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.