Recalls published in March 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in March 2026, newest first.
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Class II · 8 months ago
Roche Diagnostics Operations, Inc. cobas pro integrated solutions with cobas c 503 recall: Software defect, which allows the system to accept erroneous
Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is…
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Class II · 8 months ago
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038 recall: A potential weakness has been identified in the probe body
A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the…
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Class II · 8 months ago
Brand Name: Aesculap Product Name: Minop Trocar 150MM 4 Wking recall: There is the potential for the length of the trocar shaft to be too long
There is the potential for the length of the trocar shaft to be too long.
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Class II · 8 months ago
Staar Surgical AG EVO+ Visian recall: Toric Implantable Collamer for correction/reduction of myopia in phakic eyes
Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length…
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Class I · 8 months ago
Abiomed, Inc. Impella RP. Product Code: 0046-0011 recall: Differential pressure (dP) sensor in Impella RP devices may malfunction
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: 21GA Winged INF SET Model/ recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class I · 8 months ago
Abiomed, Inc. Impella RP with SmartAssist. Product Code: 0046-0035 recall: Differential pressure (dP) sensor in Impella RP devices may malfunction
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
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Class II · 8 months ago
Olympus Single Use Biopsy Valve. Model/ recall: Potential for rubber fragment detachment during use
Potential for rubber fragment detachment during use.
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Class I · 8 months ago
Abiomed, Inc. Impella RP Flex with SmartAssist. Product Code: 1000323 recall: Differential pressure (dP) sensor in Impella RP devices may malfunction
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
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Class II · 8 months ago
Olympus Single use Biopsy Valve. Model/ recall: Potential for rubber fragment detachment during use
Potential for rubber fragment detachment during use.
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Class I · 8 months ago
ANTHONY TRINH, 123Herbals LLC Silintan 25/pills, packaged in a 25-count bottle recall: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
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Class II · 8 months ago
Acme United Corporation Children's Healthcare of Atlanta, Instant Hand Sanitizing Wipe recall: CGMP Deviations
CGMP Deviations
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Class II · 8 months ago
Teva Pharmaceuticals USA, Inc Metoprolol Succinate Extended-Release Tablets recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 8 months ago
Acme United Corporation 1) BZK Antiseptic Towelettes 5"x7" Piedmont Sanitizing Hand recall: CGMP Deviations
CGMP Deviations
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Class II · 8 months ago
Acme United Corporation WP WipesPlus Hand Sanitizing Wipes , 5x7, 100 CT recall: CGMP Deviations
CGMP Deviations
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Class II · 8 months ago
Acme United Corporation Cleansing Towelette , 5"x 7", 1,000 case/Bulk recall: CGMP Deviations
CGMP Deviations
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Class II · 8 months ago
Teva Pharmaceuticals USA, Inc Metoprolol Succinate Extended-Release Tablets, 200 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 8 months ago
Acme United Corporation Green Guard Antiseptic Wipes , 25 wipes per box recall: CGMP Deviations
CGMP Deviations
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Class II · 8 months ago
Teva Pharmaceuticals USA, Inc Metoprolol Succinate Extended-Release Tablets, 25 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 8 months ago
Radnostix Sodium Iodide Solution, Therapeutic Oral, packaged as a) 1 ml V-vial recall: Presence of Particulate Matter: Due to production issues
Presence of Particulate Matter: Due to production issues
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Class II · 8 months ago
Mylan Pharmaceuticals Inc Amnesteem Capsules, USP 40 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class I · 8 months ago
StuffbyNainax MR. 7 SUPER 700000 capsules, 1 capsule blister card recall: Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
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Class III · 8 months ago
Cipla USA, Inc. Nilotinib Capsules, 200 mg per capsule, packaged in cartons recall: Failed Tablet/Capsule Specifications: Observed OOS results at 6-months
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual…