Health & Personal Care
HIGH
FDA DRUG
ACME United WP WipesPlus Hand Sanitizing Wipes 100 CT Recalled for CGMP Deviations (2026)
ACME United
CGMP Deviations
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DRUG
Dukal BZK Antiseptic Towelettes Recalled for CGMP Deviations (2026)
Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.
Dukal
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
First Aid Only BZK Antiseptic Towelettes Recalled for CGMP Deviations in 2026 (212,607,900 Units)
ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation for guidance.
First Aid Only BZK Antiseptic
CGMP Deviations
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 GEM PAK Recall Affects 74 Units Worldwide
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Recall 1,607 Units Worldwide (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Cartridge Recall 253 Units Worldwide (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory Recalls 7 GEM Premier 5000 Units Over PCSND Errors (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Recall for PCSND Errors in 195 Units (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 PAK Recall Affects 27 Units Worldwide (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory Recalled 180 GEM Premier 5000 PAK Cartridges for PCSND Errors (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Recall: 70 Units Worldwide for PCSND Errors (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Recall of 130 GEM PAK Cartridges for PCSND Errors (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 Recall 25 Units in 2026
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 PAK Recall Worldwide in 2026 for PCSND Warm-Up Errors
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 PAK Recall 2026 for 51 Units
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 GEM PAK Recalled for 1,629 Units Worldwide (2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory GEM Premier 5000 PAK Recalled for PCSND Warm-Up Errors (30 Units, 2026)
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory Recalls GEM Premier 5000 GEM PAK Cartridges Over PCSND Errors, 1,989 US/3
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory Recalling 10 GEM Premier 5000 PAK Cartridges for PCSND Error During Warm‑
Instrumentation Laboratory
Confirmed customer
Health & Personal Care
HIGH
FDA DEVICE
Instrumentation Laboratory Recalling 1,126 GEM PAK Cartridges for GEM Premier 5000 Over PCSND Errors
Instrumentation Laboratory
Confirmed customer
Tag Statistics
Total Recalls
2,756