All recall categories

Sterility and contamination recalls

Sterility recalls cover injectable medication, surgical and wound-care supplies and the equipment used with them. A breach of sterility does not mean anyone was harmed; it means the product can no longer be assumed safe for its use, so the notice usually asks clinicians and distributors to quarantine remaining stock.

3,093 stored notices, reported between Jun 20, 2012 and Nov 18, 2026. Newest first.

Food

Reported Aug 8, 2012

WE-24541 Vit/Min Premix Toddler (1-4 yr old) w/o DHA*ARA, NET WEIGHT 22.68 KG

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Wright Group dba Wright Enrichment, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2012

Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2012

BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bridgepoint Medical

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2012

Hidden Valley Salad Crispins Original Ranch; crisp mini-croutons, crunchy carrot bits and a blend of buttermilk and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Clorox Co. (The)

FDA (openFDA food enforcement)

Drugs

Reported Aug 1, 2012

Erythromycin Topical Solution USP, 2%, 60 mL bottle with applicator, Rx only. E. FOUGERA & CO., A division of Fougera…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Fougera Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 1, 2012

Tibial Punch Tower Assembly. Non-Sterile. CAT NO. 8000-1089. Howmedica Osteonics Corp., 59 Route 17, Allendale, NJ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Howmedica Osteonics Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2012

Oto Ease by Westone, labeled as a bacteria free, greaseless lubricant. Sold in 0.5 oz consumer sized semi transparent…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Westone Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 25, 2012

Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Nutri-Health Supplements Llc.

FDA (openFDA food enforcement)

Food

Reported Jul 25, 2012

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Standard Process, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 25, 2012

SunOpta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by SunOpta Ingredients, Chelmsford, MA 01824

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SunOpta Ingredients Group (Corporate HQ)

FDA (openFDA food enforcement)

Medical devices

Reported Jul 18, 2012

CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose driveBAY, trakSTAR, electromagnetic sensor…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Civco Medical Instruments Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jul 18, 2012

Kleenex Luxury Foam Hand Sanitizer, (Benzalkonium Chloride 0.1%), in a) 1 Liter (33.8 fl oz.), b) 1.2 Liters (40.5 fl…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kimberly-Clark Corporation

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jul 11, 2012

Microbiologics 217 Osseo Avenue North, St. Cloud, MN 56303, Gram Stain Control Slides, SLO3-10, ATCC Licensed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2012

AirLife¿ MiniSpacer¿ MDI Dispenser Adapter. Dual-Spray MiniSpacer¿ Metered Dose Inhaler (MDI) Dispenser/Adapter with 15…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Thayer Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2012

Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip Distributed by Ethicon Ethicon Inc., Somerville, NJ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2012

Pasta Roni Parmesan Cheese Flavor angel hair pasta in a Parmesan sauce with other natural flavors; Net Wt. 5.1 oz.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Quaker Foods and Snacks North America

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2012

Covidien ROTICULATOR 55-3.5 Single Use Stapler REF# 017612 The RETICULA TOR TM Single Use Staplers have applications in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LP

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 27, 2012

seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product Usage: Seprafilm Adhesion Barrier is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Genzyme Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jun 27, 2012

Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distributed: Physicians Total Care, Inc., Tulsa…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physicians Total Care, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jun 20, 2012

Murocel (methylcellulose) Lubricant Opthalmic Solution (USP, 1%), 15 mL bottle, OTC, Manufactured by Bausch & Lomb…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bausch & Lomb, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 20, 2012

T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Sterility and contamination recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Related categories

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.