Latest recalls — page 162
Older notices, newest first.
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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…
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Class II · 8 months ago
Harbin Jixianglong Biotech Co., Ltd. Semaglutide recall: CGMP Deviations This recall has been initiated due to failing to complete
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before…
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Class II · 8 months ago
Acme United Corporation Dukal BZK Antiseptic Towelette 1000 Packs per case recall: CGMP Deviations
CGMP Deviations